Beruflich Dokumente
Kultur Dokumente
EXECUTIVE SUMMARY
An examination of the issue of alien plant species invasions of the Wet Tropics
Bioregion was conducted in order to consider management implications for the
Wet Tropics of Queensland World Heritage Area. The terms of reference for the
project comprised the development of a computer-based weed Risk Assessment
System encompassing (i) inventory of existing weeds, plants presently found in
the region that may constitute sleeper weeds and plants not presently found in
the region that are proven environmental weeds in similar environments
elsewhere; (ii) prioritisation of potential environmental threat based on
explicit biogeographic/historical and biological/ecological criteria; (iii)
categorisation into management categories - eg, species targeted for prevention,
eradication and containment control; and (iv) consideration of appropriate
management actions.
This Report presents a review of Risk Assessment Systems (RASs) currently
being applied or developed with the view to formulating a robust system to screen
alien species that have naturalised within the bioregion. Systems reviewed were:
(1) RASs for Preventative Quarantine Purposes ie, International protocols (FAO
1996, 1998a, 1998b);Prevention or minimisation of risk of introductions to
countries with comparable habitats/vulnerabilities (eg, Virtue et al. in press,
Williams et al. in press); Australian protocols (Pheloung 1995, Steinke & Walton
1999); State initiatives various (eg, Hall 1999, Keighery 1999, Carter 2000); and
(2) RASs for Prioritising Existing Weed Incursions
- ie, Exotic Species
Ranking System (ESRS) of US Department of Interior, National Parks Service
(Hiebert & Stubbendieck 1993); Australian WRA Protocol Details (Pheluong
1995, Virtue et al. in press); Wildland Weed Priority Ranking System of US
Nature Conservancy (Randall et al., in press); Weed Risk Assessment in Hawaii
(Teytaud 1998; Thomas, in press); Weed Risk Assessment in the Galapagos
Islands (Tye, in press); Determination of Weeds of National Significance
(WONS) (Thorp 1999); and Weed Assessment Scoresheet of the Animal and
Plant Control Commission of South Australia (Virtue 2000). The rationale
behind the proposed Wet Tropics RAS, which was derived from existing
systems, is considered, pending its acceptance and application by the Wet Tropics
Management Authority.
The Queensland Herbariums HERBRECS list of naturalised species occurring
within the region was refined by (i) concatenating closely related taxa; (ii)
incorporating nomenclatural changes and taxonomic revisions; and (iii) by adding
those species known to have naturalised but which have not been incorporated
officially due to lack of collection, etc. This resulted in a list of at least 504
species of exotic (alien) plants that have established self-maintaining populations
in the Wet Tropics.
This Report contains a preliminary ranking, employing the proposed RAS, of
57 wet tropics weed species. These were drawn from a list of 26 terrestrial
species compiled by DNR (Land Protection), including a single native species,
supplemented with a further 24 representing a variety of other taxonomic and life
Page i
form groups, together with seven naturalised aquatics. They are thus a sample
embracing those major weeds that have already been identified by a range of
interest groups. This then is addressing an existing problem of target species for
priority control.
The two species that ranked highest were Annona glabra (Pond Apple) and
Leucaena leucocephala (Leucaena). The former is classified as a Weed of
National Significance, while the latter has demonstrated gross weedy tendencies
overseas and is among the 32 land plants in the list of the worlds 100 worst
invasive species.
Species that ranked next highest comprised: Chromolaena odorata (Siam Weed),
Sphagneticola trilobata (Singapore Daisy), Miconia calvescens (Miconia),
Hymenachne amplexicaulis (Hymenachne), Psidium guajava ( G u a v a ) ,
Thunbergia spp. (includes Blue Trumpet Vine), Mikania micrantha (Mile-aminute), Brachiaria mutica (Par Grass) and Panicum maximum (Guinea
Grass).
Several are also included amongst the worlds worst alien invaders. All have
exhibited extremely aggressive weedy tendencies elsewhere and/or are currently
extremely aggressive weeds of the region, and, in the case of Hymenachne, Par
Grass and Guinea Grass, are very aggressive and greatly impair ecosystem
function. These are considered to be transformer species ie, invasive species
that can change the character, condition, form or nature of a natural ecosystem
over a substantial area
Some consideration was given to weed management issues, although for
management there are many other considerations beyond ecological risk.
Therefore, management feasibility screening of species is argued to constitute the
next phase of the assessment process. There is some indication that others are in
the early stages of invasion (ie, prior to exponential rates of increase) and likely
constitute sleeper weeds deserving of early detection and eradication. Arguably
the first management action is to seek an embargo on further exotic species
introductions to the region and agency cooperation in the cessation of
promotion of perceived useful species such as Leucaena that already have
proven to be major environmental weeds.
The Report also presents recommendations for further research. These
include:
Page ii
1.0
INTRODUCTION
2.0
BACKGROUND
2.1
2.2
2.2.1
2.2.2
2.2.3
2.3
2.4
3
6
7
7
8
10
2.5
INVASION ECOLOGY
SUBJECT AREA
CLIMATE
PHYSIOGRAPHY, GEOLOGY AND SOILS
LANDSCAPE CONFIGURATION AND NATIVE VEGETATION COVER
CONSIDERATION OF PECULIARITIES OF THE HOST ENVIRONMENT
PREVIOUS CONSIDERATION OF WEEDS WITHIN THE WET TROPICS
BIOREGION
CONSIDERATION OF LANDSCAPE COMPONENTS AT RISK
3.0
15
3.1
3.1.1
3.1.2
3.1.3
3.1.4
3.2
3.2.1
3.2.2
3.2.3
3.2.4
3.2.5
3.2.6
3.2.7
3.3
13
14
4.0
TAILORING A WEED RISK ASSESSMENT SYSTEM FOR THE WET
TROPICS BIOREGION
36
4.1
37
Page iii
4.2
4.3
4.4
37
38
40
5.0
EVALUATION OF PLANT SPECIES NATURALISED WITHIN THE
WET TROPICS BIOREGION
5.1
5.1.1
5.1.2
5.2
5.2.1
5.2.2
5.2.3
44
44
44
44
46
47
49
50
5.3
5.4
5.5
5.6
50
53
53
55
55
6.0
57
6.1
6.2
6.3
6.4
57
58
59
6.5
7.0
62
5.2.4
60
61
BIBLIOGRAPHY
64
A1-1
A2-1
(CD)
Page iv
Biological diversity faces many threats throughout the world. One of the
major threats to native biological diversity is now acknowledged by scientists
and governments to be biological invasions caused by alien invasive species.
The impacts of alien invasive species are immense, insidious, and usually
irreversible. They may be as damaging to native species and ecosystems
on a global scale as the loss and degradation of habitats.
SSC Invasive Species Specialist Group of IUCN (2000)
Page v
1.0
Introduction
Lvei (1997:627), noting that the scale of species introduction has vastly increased,
argued that alien species invasion must be recognised as an important component of
human-induced global change and as a serious threat to biodiversity. Introduction of
alien organisms frequently produces drastic impacts on the receiving biota and
systems. Long term global effects comprise both decreasing the local distinctiveness
of floras and faunas and the breaking down of geographic isolation that promotes and
maintains global biodiversity generally. In fact, Willis et al. (2000:275) claim that
threat to biodiversity posed by alien species invasions is second only to habitat loss.
It is estimated (Virtue et al. in press) that approximately 15% of the vascular flora of
Australia (or over 2 200 species) has been introduced. Those introductions have been
both deliberate (ie, for purposes of agricultural production, ornamental amenity and for
other reasons) and accidental (as in contaminants in imported pasture seed or stock, via
various modes of human transport, and the like). A significant subset of these exotic
species has subsequently naturalised in the new host environment to impose major
impacts on Australian ecosystems, both natural/semi-natural and anthropogenic
(including intensive agro-ecosystems and extensive rangelands). These subsets are
referred to as environmental and agricultural weeds respectively.
The vascular flora of the Wet Tropics Bioregion alone, is estimated to be 4 664 species
(WTMA 2000:25). With a total of 508 exotic taxa noted by the Queensland Herbarium
to be naturalised within the region (see Appendix 2 below) which itself is a likely
underestimate (see Section 5.5.1) this amounts to almost 11% of the regions native
flora. Despite the exotic component being a slightly lower proportion than the national
average (Virtue et al., in press), the existence of a high level of endemism and the fact
that much of the region (approximately 9 000 km2) has been inscribed on the World
Heritage list as the Wet Tropics of Queensland World Heritage Area (Werren & King
1991) predicates a high priority on weed control within area management. This has
prompted the present initiative for the development of an environmental weed risk
assessment system (RAS) for the Wet Tropics Region as a means of contributing to
the meeting of Australias international obligations under the World Heritage
Convention. The RAS will incorporate an ecologically based, logistically and
economically feasible system for identifying priorities for weed prevention,
eradication, containment or control.
While there are many pests of the agricultural and pastoral industry and others
(particularly ponded pasture species) that constitute both pests of agricultural and
natural systems, it is the environmental weed component that is the subject of the
current investigation. Environmental weeds are defined as introduced species
capable of establishing, or are considered to have a high probability of establishing
self-sustaining populations by invading native communities or ecosystems and are
capable of causing major modification to species richness, abundance or ecosystem
function (Goosem 1993). Williams & West (2000:429) note that these can come in all
shapes and sizes, and grow in all niches in an ecosystem. This component includes
(i) plants that have already demonstrated a capacity to institute such changes within the
region and (ii) others that occur in the region and, due to certain inherent traits or
because of their demonstrated weediness elsewhere, constitute potential threats to native
communities and ecosystems. The latter might be referred to as sleeper weeds (Groves
1999).
Page 1
Page 2
2.0
Background
The current study was recently commissioned by the agency responsible for
overarching management of the Wet Tropics World Heritage Area ie, the Wet
Tropics Management Authority (WTMA). Day-to-day management of the Area is the
responsibility of State partner agencies that include the Environment Protection
Authoritys (EPA) Queensland Parks and Wildlife Service (QPWS), Department of
Natural Resources (DNR) and others. What follows is designed to inform WTMA
decisions regarding allocation of priorities and resources to weed control within the
wider gamut of area management and management activities of partner agencies.
2.1
Invasion Ecology
Invasion issues came to the forefront of a developing natural science with the
publication in 1958 of Eltons seminal book called The Ecology of Invasions by
Animals and Plants. This prompted not only an interest in plants and animals that
have impacts on agriculture but also a greater scientific emphasis on the rapid changes
that increased biotic exchange was imposing on indigenous systems and the adverse
implications for the survival of native species.
Investigation of exotic species invasions was complemented by the work of Grime
(1977) who identified three primary reproductive strategies in plants and discussed the
theoretical ramifications for ecology and evolution. He linked external factors such as
stress and disturbance and considered the four permutations of (i) high stress-high
disturbance, (ii) high stress-low disturbance, (iii) low stress-low disturbance and (iv)
low stress-high disturbance and determined that only three provided viable plant
habitats since the first scenario is inhospitable to plant growth. Accordingly, scenario
(ii) is associated with stress-tolerant plants, (iii) with competitive plants, and (iv)
with ruderal or annual plants that are physiologically/reproductively adjusted for rapid
life cycles attuned to regular or periodic disturbances. It is the latter category that
provides most of the known agricultural weeds ie, plants that can cope with, or are
advantaged by, disturbances associated with cultivation and/or grazing. Environmental
weeds, however, belong predominantly but not exclusively to groups of plants
associated with scenario (iii). These are species with superior competitive abilities
including rapid and highly plastic stress responses (Grime 1977:1184) or such as may
arise from the lack of natural enemies in the novel environment (Markin 1989:70) that
tend to maximise vegetative growth.
Competitive superiority can arise from various biological/autecological attributes. For
instance, rapid acclimation to sudden light increases brought about by canopy gap
formation is demonstrated to advantage exotic tree species establishment in subtropical
island forests of Japan (Yamashita et al. 2000). Incidentally, the tree species in
question, Java Cedar (Bischofia javanica) is a native rainforest tree of the Australian
Wet Tropics. It exhibits a capacity for superior performance in photosynthetic rates of
existing shade leaves and rapid deployment of new sun leaves when transferred from
shade to sun commensurate with an ability to outperform natives in habitats prone to
typhoon (cyclone) disturbance.
Heywood (1989:44-45) argues that invasion of tropical forests is triggered by
widespread disruption or conversion of the primary forest to secondary successional
communities. The history of widespread logging of the rainforests, combined with
cyclone disturbance, has brought about such a situation regionally and, accordingly, an
increase in invasion proneness.
Page 3
Genetic screening may offer possibilities for weed detection since it appears that some
non-indigenous plant species grow taller and exhibit a higher reproductive capacity in
a host environment compared with their performance in the native environments.
Willis et al. (2000) investigate the possibility that this is more of a genetic change
rather than the traditional proposition of a plastic response to a benign new
environment. By comparing several weeds in Australia and New Zealand with their
counterparts in Britain and continental Europe these workers failed to find evidence
that increased plant size, where it occurs, is a genetically determined characteristic of
of invasive plants, or that the phenomenon is widespread among invasive species
(Willis et al. 2000:282). It is, thus, more likely to be a plastic response to a novel
environment.
Chemical defences are also associated with the frequently observed superior
performance of alien plant species. These defences may be in the form chemical
agents such as those that occur in the Neem Tree (Azadirachta indica) that reduce
herbivory, therefore maximising photsynthetic sequestration and growth. Callaway &
Aschehoug (2000) and Ridenour & Callaway (2001), in studies of root exudates of a
noxious weed in America, have demonstrated a much greater negative effects on
American native grasses than on their counterparts in communities from which the
weed originates. In commenting on this work, Jensen (2000:421) claims that the
invader apparently gains an edge in its adopted home not only by ditching its
herbivores but by wielding [chemical] weaponry that hampers its new neighbors
(sic) growth. This has significant repurcussions regarding competition for resources
and, of course, implications for invasiveness potential.
Davis et al. (2000) attempt to replace andectodal study of the invasion process by
considering the availability of resources to a potential invader. These workers suggest
that invasion is influenced by three major factors: ie, (i) propagule pressure (the
numbers of seeds/fragments, repeated introductions, etc.), (ii) characteristics of the
introduced species, and (iii) the invasibility of the new (host) environment. While the
second factor pertains to intrinsic or biological traits of the prospective invader, the
third is an emergent property that derives from climate, disturbance regimes and the
competitive abilities of resident plants. They further argue that a more integrative
approach to invasibility and the invasion process might be proposed with respect to
fluctuating resource availability. The proposition is that a plant community becomes
more susceptible to invasion whenever there is an increase in the amount of unused
resources (Davis et al.2000:529) and that a communitys suceptibility to invasion is
not static.
Disturbance whether regular or episodic is a natural feature of dynamic ecosystems
(Sousa 1984) but also facilitates the invasion process by eliminating/reducing the cover
and/or vigour of native competitors and/or by increasing resource levels. This is
especially so when it coincides with ready availability of the invading species
propagules. Consequently, the following predictions can be made:
Page 4
invasability will increase when the interval is long between increase in resource
supply and eventual capture/recapture of sites by native vegetation;
nutrient-rich communities, in particular, that are subjected to increased grazing
pressures are suceptible to invasion;
there is no necessary relationship between the species diversity of a plant
community and its resilience to invasion; and,
there will be no general relationship between the primary productivity of a
community and its susceptibility to invasion (Davis et al. 2000:532).
Page 5
In a review of exotic plant species in Hawaii, Smith (1989:61-62) also details five
major impacts in comparable tropical landscapes other than simple physical
displacement of native species. These are (i) formation of monotypic stands that
results in biodiversity loss and can have devastating effects on the survival of endemic
species with limited ranges and small population sizes; (ii) changing fire characteristics
(especially due to fire-promoting exotic pasture grasses); (iii) changing soil-water
regimes (often due to lack of phenological synchronicity with host environments
climate); (iv) changing nutrient status (associated with introduced N-fixing pasture
legumes); and (v) promotion of mutually beneficial interaction between alien plants
and feral animals. Also, it should be recognised that impacts can amplify as the
cumulative effects of multiple, low probability events (Levins 1989:426).
King (1987) reviewed the multiple-staged process of extinction and identified 13
milestones the final being excessive competition from introduced species that are
eventually responsible for pushing organisms irretrievably over the edge. Incidentally,
an earlier milestone was hybridisation and genetic swamping that may be due to
exotics as well as translocated natives. Within Australia, invasive exotic species have
been primarily implicated in the presumed extinction of at least four plant species and
have the potential to force many more native plants to extinction (Groves & Willis
1999:164). The highly restricted nature of many endemic plant species distributions
within the Wet Tropics Bioregion (Werren et al. 1995; Goosem et al. 1999) renders
this regional flora particularly vulnerable to extinction due to threatening processes
such as pest invasion.
It must be noted, however, that the impacts on native biodiversity associated with alien
invaders are not exclusively negative. Groves & Willis (1999:169) point out that
impacts can, in fact, be positive, negative or neutral, depending on the biotic group
measured. A tropical example ie, that of the invasion of Mimosa pigra into
wetlands of the Northern Territory was employed. This showed that some plant
groups, birds and lizards sustained negative biodiversity impacts, but positive benefits
were felt by the rare marsupial mouse Sminthopsis virginiae and no changes in frog
numbers were detected. It is evident that some invasive exotic species in the wet
tropics also produce some benefits to at least nectarivorous native insects, given
numbers of butterflies observed foraging on Lantana camara and Asclepias
currasavica. There are, however, strong indications that specialist host-specific insects
are impacted greatly with the replacement of native vegetation with exotics supporting
greatly reduced arthropod numbers with significant repercussions for predatory mites,
spiders, wasps and other parasitic insects and insectivorous frogs, reptiles, birds and
mammals (McFadyen 2000).
2.2
Subject Area
The Wet Tropics Bioregion is situated along the tropical east coast of northern
Queensland. Its western boundary is shared with the Einasleigh Uplands Bioregion,
which lies in the rainshadow of high and wet coastal ranges that dominate the Wet
Tropics. In the north the region is bordered by the eastern part of Cape York
Peninsula, and in the south grades into the northern coastal extremity of the Brigalow
Belt. With an area of 1 849 725 ha, the Wet Tropics Bioregion covers approximately
1% of Queensland (Goosem et al. 1999:7/5).
The region is distinguished among Australian bioregions by the extraordinary richness
of its flora and vegetation. It is recognised as one of the worlds centres of plant
diversity (Werren et al. 1995) and supports the most extensive tracts of closed forest
Page 6
(vine forest or rainforest) on the continent. It is the second most floristically rich1 of
Australias biogeographic provinces with in excess of 4 660 species recorded (WTMA
2000:25) of which 25% or over 1 150 species are endemic. The level of generic
endemicity in the Wet Tropics Bioregion is second only to New Caledonia in terms of
endemic genera conserved per unit area (Webb & Tracey 1981, Morat et al. 1986).
In addition, many terrestrial vertebrates are known from the Wet Tropics Bioregion
(Williams et al. 1996). Of these, 20 are introduced. Excluding these, the total of 566
species represents 28% of all Australian terrestrial vertebrates. At least 12% of these
are endemic (i.e., entirely restricted to the region), although this is highly variable
between taxonomic groups (4-39% - Williams et al.,1996). The region also supports a
rich freshwater fish fauna, with 40% of the Australian species complement
represented here, and the Russell-Mulgrave system, in particular, being extraordinarily
important to this group (Pusey, pers. comm.). In addition, the invertebrate fauna is
very diverse. This is indicated by the fact that 60% of the total Australian species
within a single invertebrate group - the butterflies - occurs within this region. Such
faunal diversity is similarly threatened by invasive alien species, including both plants
and animals.
2.2.1 Climate
Many of the distinctive features of the region relate to the high rainfall and terrain
diversity. The mean annual rainfall ranges from about 1 200 mm to over 8 000 mm.
However, Mt Bellenden Ker, at an altitude of 1 561 metres, has recorded as much as 10
472 mm over an eight month period (during January to August 1979) and has received
1 140 mm of rain in a 24 hour period (Tracey 1982). Rainfall intensities at this station
are amongst the highest recorded in the world. The rainfall is distinctly seasonal with
over 60% falling in the summer months of December to March. By comparison with
other tropical rainforested areas of the world, the wetter parts of the region lie at the
'extremely wet' end of the hydrological spectrum. The occurrence of widespread
overland flow also appears to be rare in wet tropical rainforests elsewhere.
Intense tropical cyclones are a natural disturbance feature of the region's climate, with
an average of one severe cyclone occurring every three years. This region has the
highest incidence of such tropical cyclones with over 40% of all systems so classified
impinging on the Wet Tropics. This is a major factor shaping the structural and
floristic differentiation of the vegetation - particularly with respect to the mosaics of
the coastal lowlands (Werren et al. 1995).
The coastal belt experiences a mean daily temperature from a January maximum of
31oC to a minimum of 23oC with a 5Co reduction in these figures during a very mild
winter. The uplands/tablelands are cooler with mean daily temperatures ranging from
28oC to 17oC with mean daily winter temperatures ranging from 22oC to 9oC.
2.2.2 Physiography, geology and soils
The uplands or tableland unit consists of undulating country at an altitude of around
900m, with rounded summits rising to more than 1 200m. The highest peak is Mt
Bartle Frere which reaches 1 622m. To the east of the tablelands the Eastern
Escarpment marks the limit of headwards erosion into the uplifted erosion surface from
the coastal lowlands. This is a unit typified by rugged topography, rapid geomorphic
1
The south-western province of Western Australia is the foremost species-rich region of Australia with an estimated
5 500 species (Beard 1995:484), although the generic and familial diversity of the Wet Tropics far exceeds that of this
region.
Page 7
notophyll vine forest - rarely without Acacia spp. (types 7a, 7b)
Page 8
Each forest type can be correlated with climatic type, soil parent material, altitude and
disturbance regimes. The floristic composition within each type varies from one
locality to another and reflects, amongst other things, past expansions and contractions
of rainforests due to climatic perturbations.
Rainforests attain their peak development as complex mesophyll vine forests on the
very wet and wet lowlands and foothills where parent materials range from basalts,
basic volcanics, mixed colluvia and riverine alluvia. These communities exhibit an
uneven canopy extending to between 20 to 40 metres and there is much stratification
and many emergents with large spreading crowns (eg, figs, Ficus spp.). Floristic
composition and variety of life forms are the most complex of any terrestrial vegetation
type on the continent. Exposed sites such as foothill ridges and seaward slope facets
often exhibit cyclone disturbed or broken canopies with 'climber towers' and dense
vine tangles. These are locally known as 'cyclone scrubs' (Webb 1958). These systems
appear vulnerable to exotic species infestations, especially along edges adjacent to
agricultural lands. Within complex mesophyll vine forest communities variation in site
factors induces conspicuous structural differentiation such as the increase in palms on
sites with impeded drainage and gingers and aroids in gullies and along creek banks
which are permanently saturated with water (Tracey 1982).
The notophyll vine forest category embraces a structurally and floristically diverse
group of communities (types 5, 6, 7, 8 of Tracey 1982). These occur on small areas of
basic volcanic parent materials on cool wet uplands and highlands (ie, type 5a) and on
a range of drier sites at various elevations (type 5b), the western and northern fringes
of the main rainforest massif from Cardwell extending to Julatten, the Hann Tableland
and to the north of Bloomfield (type 6), on sandy beach ridges in drier coastal zones
and exposed sites backed by foothills north of Cairns (type 7), and as one of the most
extensive, an even-canopy mountain forest assemblage (type 8) on granitic ranges
rising from 400 to 1 000 metres altitude between Ingham and Cooktown. These
communities, while extraordinarily variable, are characterised by a canopy range of 1245 metres in height, the occurrence of rattans or palm lianes, strangler figs, frequently
conspicuous epiphytes and variable amounts of ferns, walking stick palms (Linospadix
spp.) and fleshy herbs.
Towards the upper end of the altitudinal spectrum on the summits and upper slopes of
the higher peaks which are frequently enshrouded by cloud (hence horizontal
interception or 'fog-drip' is characteristic) and often exposed to strong winds, simple
microphyll fern forests or thickets dominate. These often possess a strong aerially
suspended moss component and are sometimes referred to as 'cloud' or 'elfin' forests, or
more precisely 'wet montane forests'.
Many sites experience significant water stress during the dry season and support closed
forest/thicket communities characterised by the occurrence of taxa which are semideciduous to deciduous. Semi-deciduous mesophyll vine forest (type 4) is restricted to
minor occurrences to the north-west of Cairns, and to foothills between the Bloomfield
River and Cooktown (Tracey 1982). Sporadic occurrences of deciduous microphyll
vine thicket (type 11) occur on fire-free rocky sites and exposed headlands.
Constituents are mainly multi-stemmed and fully deciduous. Vine forest with
sclerophyll emergents (types 12, 13) are also encountered. These represent different
stages of post-disturbance (eg, fire, logging and/or cyclones) succession and vary
considerably in floristic composition, with each sub-type characterised by the
dominance/co-dominance of certain sclerophylls (ie, eucalypts and wattles).
Page 9
The Wet Tropics of Queensland is distinguished by virtue of the fact that in 1988, as an
initiative of the Commonwealth Government, some 9 000 km2 of this bioregion have
been inscribed on the World Heritage List (Werren & King 1991). This means that
Australia has entered into an international agreement to protect, conserve and present
the area's World Heritage values for present and future generations. This constitutes an
international obligation to protect those outstanding universal natural (and cultural)
values for which the Area was listed. These values relate to the four criteria for listing
an area ie:
It is easily demonstrated that these values are concentrated in the native vegetation
communities and that their protection, conservation and presentation is reliant upon the
ongoing integrity of these systems. Clearly, weed invasion represents a threat to this
and is identified as a pressure affecting condition that warrants a management
response (in Condition, Pressure, Reponse models) and as a threatening process to
the survival of threatened species and REs (WTMA 1999:22). Those REs at risk are
listed in Table 2.
The tropicality of the region ie, its warm to hot, humid climate is a situation that
can be exploited by alien plant species, particularly species adapted to similarly warm,
moist climatic conditions. Conditions so conducive to rapid plant growth can greatly
accelerate the invasion process. Rejmnek (1989:383) clearly demonstrates that plant
communities in mesic environments are more invasible compared with those in more
extreme environments.
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Table 2: Wet Tropics Regional Ecosystems at risk (after Goosem et al.1999:Table 7.4)
Summary of conservation status
Endangered
24
Of concern
17
No concern at present 64
TOTAL
105
Endangered Regional Ecosystems
7.2.1
7.2.2
7.3.1
7.3.2
7.3.3
7.3.4
7.3.6
7.3.7
7.3.10
7.3.12
7.3.13
7.3.22
7.3.24
7.3.25
7.3.26
7.3.28
7.8.2
7.8.3
7.8.6
7.8.7
7.8.8
7.11.2
7.11.8
7.12.12
The region also is characterised by high local relief exceeding 1 600m and its
ecological diversity, promotes mostly year-round plant growth in a range of
environments. This range of conditions, from tropical analogues of cool temperate
forests and high montane summit areas, through hot-dry tropical open woodlands to
very wet tropical lowland communities, is present, allowing a commensurate range of
environments for the establishment of an array of alien plants.
Page 11
The subject area is highly biodiverse (Werren et al. 1995, WTMA 2000). High
biodiversity means that a large number of resident organisms are present that might
present a hindrance to weed establishment, or, on the other hand, that can pollinate
and/or disperse an alien species (Orians 1986:135) potentially facilitating its invasion.
It is generally contended that intact forested areas particularly those that are highly
biodiverse are particularly resistant to weed invasion (eg, Humphries & Stanton
1992). However, this contention is not supported by the work of Higgins et al.
(1998:303) in Cape Peninsula, South Africa, which indicates that species richness and
invasibility are positively correlated and that species richness is a poor indicator of
invasive resistance in the study site. Further, they argue soundly for spatially
explicit approach to quantifying threats to biodiversity as the basic information
required to prioritise threats from alien species and the sites that need urgent
management attention. Similarly, Lavorel et al. 1999:41) demonstrated that there was
no strong relationship between invasibility and functional or species richness.
Such conflicting understandings arising from both anecdotal information and intensive
scientific study of particular groups of weeds at particular locations are as problematic
as the paradox of weed invasion itself. Sax & Brown (2000:363) note that it is
paradoxical that exotic species invade and displace native species that are well
adapted to local environments and go on to offer an explanation of the invasibility of
continental regions that is a function of pre-adaptation to human-modified
environments and escape from co-evolved enemies. In contrast the greater
invasibility of islands is considered to reflect the peculiar evolutionary dynamics of
insular species.
The greater susceptibility of island habitats to alien invasions is well documented
(Heywood 1989, Rejmnek 1989, Lvei 1997, Sax & Brown 2000, Thomas in press).
Various workers, have commented on the natural insularity of many Australian
rainforest patches, coining phrases such as islands in a sea of sclerophyll vegetation
(Webb & Tracey 1981), or islands of green in a land of fire (Bowman 2000). It is
reasonable to assume, therefore, that increased susceptibility to invasion is associated
with such a spatial configuration.
Moreover, the extent of fragmentation of a variety of vegetation types within the
region, including non-rainforest communities, is great. This includes the
disproportionate loss of wetlands (Russell et al. 1996) and priority coastal
communities of the FNQ 2010 Plan. It is notable that Groves & Willis (1999:164)
argue that increasing fragmentation of natural vegetation is a major factor that allows
weeds to establish and dominate and thereby threaten still further the continued
existence of native plant species and the Australian ecosystems in which they occur.
Given the above, we are clearly contending with a situation equivalent to the title of a
paper by Timmins & Owens (in press) ie, scary weeds and superlative places.
Those superlative natural values that justified inscription of much of the region on the
World Heritage List are potentially at risk from a suite of highly invasive alien weeds
that exceeds 500 species. The task, therefore, of determining the aggressive invaders
amongst the host of alien plant species introductions is a vital but daunting one. Based
on studies of what traits might confer invasive potential among closely related species,
Radford & Cousens (2000:531) even suggest that invasiveness is essentially
unpredictable. What is evident, however, is that both intrinsic biological and host
environmental factors are involved and that it is dependent on some habitat/plant
specific interactions between a prospective invader and location of the introduction.
Page 12
2.4
Just after its inception, WTMA commissioned a comprehensive review of the regions
weeds that was undertaken by Humphries & Stanton (1992). These workers
considered that large tracts of rainforest did not appear to be particularly vulnerable to
significant weed incursions even after natural disturbance but that riparian systems,
freshwater wetlands and paperbark swamps were being extensively invaded by a suite
of major environmental weeds. Eight of these weeds were identified as being of
priority concern due to their capacity to spread into intact communities without being
assisted by human disturbance. These are Annona glabra, Clitoria laurifolia, Coffea
arabica, Harungana madagascariensis, Lantana camara, Sanchezia parvibracteata,
Thunbergia grandiflora and Turbina corymbosa. A subset (5) of these was considered
particularly problematic and consultancies were offered to Swarbrick (1993a, 1993b,
1993c) and Swarbrick & Skarratt (1994) to investigate extent of infestations, potential
areas of infestation and options for control. The concerning subset comprised
A. glabra, H. madagascariensis, T. corymbosa, S. parvibrateata and C. arabica.
Mechanical and chemical control trials were also undertaken to produce
recommendations for treatment.
Subsequently, intensive control efforts targetting Harungana were implemented
resulting in control of around 60% of the infestations (Walton pers. comm.).
Unfortunately, resources were not allocated to extend treatments and to provide
follow-up so infestations have rebounded and the weed continues to invade forests
along the eastern fall of the Bellenden Ker massif and along the Graham Range.
Pond Apple a species that has been elevated to a Weed of National Significance
(WONS) - has been subjected to strategic control within only one sensitive protected
area to date. This is Eubenangee Swamp National Park where a combination of
mechanical, chemical and fire management treatments have been applied by QPWS
staff. The invasive vines, Thunbergia grandiflora and Turbina corymbosa have also
been subjected to strategic control; the former by QPWS staff in Mulgrave River
National Park in concert with Pest Management crews of Cairns City Council (CCC),
and the latter within Kamerunga Conservation Park by CCC personnel.
The discovery in 1994 of Siam Weed (Chromolaena odorata) in the Mission Beach
area and later as significant infestations along the Tully River led to a major
Commonwealth initiative aimed at its eradication. A nationally funded joint effort led
by DNR entitled a Strategic Weed Eradication and Education Program (SWEEP) was
instigated, with major infestations treated and monitored. A follow-up treatment and
monitoring program remains current in Cardwell Shire and nearby parts of Johnstone
Shire where outbreaks were documented.
Currently, weed control is practiced throughout much of the region by the cane
industry (Cane Pests & Productivity Board) along with individual landholders. These
efforts primarily target agricultural weeds (cf. BSES 1989) although some can also be
invasive of other land uses including conservation. More integrated efforts are
expended by local government pest management and environmental repair (ie, Wet
Tropics Tree Planting Scheme) crews. DNR Land Protection officers assist this
activity through provision of advice on priorities, control treatment and by extension
work generally. Research on both weed autecology and chemical control are underway
at DNRs South Johnstone research centre. There is some involvement of the
Rainforest CRC in these ventures, along with this current initiative.
Page 13
2.5
As argued by Humphries & Stanton (1992:viii), riparian systems and wetlands have a
very high functional significance yet are particularly vulnerable landscape features to
weed invasion. Pysek & Prach (1993) document the high susceptibility of riparian
vegetation elsewhere in the world to invasion by exotic plants. Baker (1986:48) also
confirms this and other workers such as Dcamps et al. (1988, 1995) also discuss this
issue in detail. They also report on the enhancement of exotic species invasion of such
systems when human-induced disturbances significantly modify the hydrologic regime.
In the Mackay district of the Central Queensland Coast that is often referred to as a
southerly outlier of the Wet Tropics proper, Batianoff & Franks (1998:123) specified
riparian forest as the most susceptible vegetation type to environmental weed
invasion and that disturbed habitats support 95% of the environmental weeds.
Both riparian systems and wetlands have been disproportionately lost and degraded
within the Wet Tropics. The condition of the regions wetlands varies greatly and a
great proportion - estimated from 1992 aerial photography to be 46% of their recorded
extent in 1952 in the centrally located Russell-Mulgrave Catchment alone (Russell et
al. 1996:13) - have been drained and lost. Lagoons have been filled and turned into
canefields with their feeder streams and flowpaths transformed into cane drains, with
many conduits for the march of Pond Apple and many other weeds across the
landscape. Ewel (1986:222) notes that drainage of, and dike construction within, the
northern reaches of the Everglades marshes rendered them more invasible.
As a result, the regional ecosystems (REs) associated with these features have become
correspondingly rare and/or threatened (see Table 2 above). They too can be
considered to be at further risk from threatening processes, among which are those
posed by exotic plant and animal invasion. These considerations are incorporated in
components of the proposed RAS in Section 4.3, below.
In addition, there are some 363 species of plants within those communities that are at
rare and/or threatened (Goosem et al. 1999:7/60). Weed invasion may constitute a
threatening process in some situations where Pond Apple is replacing paperbark
wetlands that support the vulnerable Ant Plant (Myrmecodia beccari) which, in turn,
hosts the ant larval symbionts of the endangered Apollo Jewel Butterfly (Hypochrysops
apollo apollo).
It is not known exactly which species of animals are specifically at risk from weed
invasion. In fact, in certain circumstances, the proliferation of rank exotic grasses has
advantaged some species such as the vulnerable Crimson Finch (Neochmia phaeton
phaeton). McFadyen (2000) argues strongly that the ongoing habitat degradation
associated with weed invasion, however, does pose considerable risks to survival of a
host of animal species. She demonstrates that alien plants displace native flora on
which an entire complex native food web is dependent. They can, as in the case of
exotic species of Aristolochia, contain toxins that kill host-specific native species such
as the Cairns Birdwing Butterfly (Ornithoptera priamus euphorion) that deposit eggs
on native species (eg, A. tagala), or may be unpalatable to generalist herbivores, thus
decreasing food resources. Similarly, nectarivores can be greatly impacted with the
displacement of nectar-producing native plants resulting in the disruption or
displacement of guilds of organisms. The point is made that there are great flow-on
effects, many of which are entirely unpredictable.
Page 14
3.0
Various authorities throughout the world employ a variety of pest risk assessment
systems' (RAS) for two basic purposes. The first is to minimise the risk of introduction
of invasive alien organisms and is the province of international trade (eg, International
Standards for Phytosanitary Measures FAO 1996, 1998a, 1998b), quarantine and
national border control. The second, which is more relevant to the present task, is
related to prioritising established pest species for control, including the detection of
naturalised exotic species in their early stages of invasion that may constitute future
major weed problems. The two approaches share many elements, therefore both types
of approach may have relevance to the formulation of a risk assessment system (RAS)
for the Wet Tropics Bioregion and consideration of each is warranted.
3.1
Pest risk assessment was originally designed primarily to avoid importing pest
organisms and, with the great increase in global trade, is increasingly a focus of
quarantine and trade control authority activity. The Australian Quarantine Inspection
Service (AQIS) has a major responsibility to ensure that further introduction of pest
species to this country is kept to an absolute minimum. This organisation employs a
RAS to screen proposed plant imports and to provide an early warning system of
potential pest species and source areas. Individual states also influence the process of
screening proposed plant and animal introductions.
Risk assessment is fundamental to any initiative aimed at reducing the chance of weed
introductions. Waterhouse & Mitchell (1998), in setting out target species for
monitoring and survey associated with the Northern Australian Quarantine Strategy,
rely upon recorded weediness in the literature. Factors such as that associated with a
plants weediness elsewhere are usually the first filter in such introduction-screening
protocols.
Species purportedly not yet present in Australia but which are recorded in
neighbouring countries are ranked according to (i) potential to have serious economic
impacts, (ii) potential to have significant environmental impacts, (iii) likelihood of
accidental dispersal from adjacent land masses, (iv) a history of rapid recent spread in
Indonesia or Papua New Guinea, and (v) likelihood of successful establishment in
northern Australia (Waterhouse & Mitchell 1998:10). The resultant list of 41 species
includes two (ie, Chromalaena odorata and Mikania micrantha) that pose very serious
threats and which have been recorded within the Wet Tropics region. Both have been
subjected to intensive control measures.
3.1.1
Organisations such as the IUCN and FAO now clearly recognise the major threat posed
by alien species invasions to the worlds biodiversity. The Invasive Species Specialist
Group of the former claims that impacts of alien species are immense, insidious, and
usually irreversible [and] may be as damaging to native species and ecosystems on
a global scale as the loss and degradation of habitats (SSC 2000:1). Accordingly, the
Food and Agricultural Organisation (FAO) of the United Nations has set in place
various protocols to address such threats.
Guidelines for Pest Risk Analysis (PRA) were published by the FAO in 1996. These
cover (i) PRA process initiation, (ii) the risk analysis process itself, and (iii) managing
pest risk (FAO 1996:6). The second of these stages of the process (PRA) is of direct
Page 15
relevance to the present task. After identification of a pest, this second stage examines
individual pests to evaluate whether the criteria for quarantine pest status are
satisfied. These cover pests of potential economic importance (FAO 1996:11),
considering geographical distribution, biology and economic importance, and is reliant
on expert judgement in the assessment of establishment, spread and economic
importance potential. If this assessment suggests that a pest has significant economic
importance and introduction potential then quarantine protocols for risk management
are set in train. These cover a range of options (eg, inclusion on lists of prohibited
pests, inspection and certification prior to export, inspection at entry, etc. FAO
1996:16). They also provide for a process of monitoring and evaluating the various
options in relation to this pest. Subsequent guidelines cover protocols for the
determination of pest status in an area (FAO 1998a) and guidelines for pest eradication
(FAO 1998b). These guidelines are currently established under the name of
International Standards for Phytosanitary Measures (FAO 1999) and fall under the
auspices of the International Plant Protection Convention. It is notable that the
economic component of PRA includes effects on ongoing integrated pest
management (IPM) programmes, environmental damage, capacity to act as a vector
for other pests, inter alia (FAO 1999:11, emphasis added).
3.1.2
various plant traits should be fairly easy and quick to determine (ie, selfcompatability and number of seeds per plant may be not easy to establish and
can be avoided);
(ii)
(iii)
(iv)
the positive traits (eg, utility as stock forage, ornamental amenity) should be
considered quite separately from invasive potential;
(v)
(vi)
Weed protocols remain state-based in the U.S.A. and generally focus upon dealing
with existing pest problems (eg, Hiebert & Stubbendieck 1993).
Page 16
Thomas (in press) comments upon weed RAS development in Hawaii, which, in many
aspects hosts similar environments to those existing within the Wet Tropics Bioregion.
Invasive species entry prevention is a hot topic in Hawaii, with importation
essentially agriculture-based (Thomas in press:43, Mitchell pers. comm.). It is likely
that elements of the Hawaiian weed RAS (Teytaud 1998) such as are under
development under the auspices of a project dubbed HEAR Hawaiian Ecosystems at
Risk. Nominally it is an asset based (sensu Hall 1999:82) approach but it has will
have significant implications for quarantine protocols, especially assessment of
intrinsic attributes after Cronk & Fuller (1995) (see Section 3.2.4 below) and should be
compliant with IUCN Guidelines for the Prevention of Biodiversity Loss due to
Biological Invasion (Thomas in press:44).
Protocols associated with weed risk assessment operating in New Zealand are
informative, particularly with respect to aquatic weed risk assessment (Champion &
Clayton, in press). It is notable that those that were developed by New Zealands
Department of Conservation underpin weed risk assessment in other places such as
Galapagos Islands (Tye in press:25) and has been considered in RAS development in
Hawaii (Thomas in press).
3.1.3
Page 17
They were constrained by their lack of flexibility. The ability of the WRA system to
make reliable recommendations has a sound quantitative basis, and the mechanism is
transparent. These features are basic requirements for establishing phytosanitary
conditions in accordance with the General Agreement on Tarrifs and Trade (GATT)
SPS agreement.
Table 3: Scoring system employed by AQIS for decision-making on the importation of plants
(after Hazard 1988 in Pheloung 1995)
Criterion
Points
1:
Page 18
State, including in all ten2 local government areas within the bioregion. In the PMP
process, both weeds of agriculture and environmental weeds that occur within each
local government area are considered and ranked according to agricultural and/or
environmental risk and control potential. This allows the targetting of weeds of
highest priority that are considered to be controllable so that limited resources can be
strategically allocated in Councils works programs.
In order to rank those species of highest priority for research, staff of the Alan Fletcher
Weeds Research Institute have collated those listed in the regions local government
PMPs and have utilised a Multi-Objective Decision Support System (MODSS)
(Bebawi pers. comm.). This excercise resulted in the ranking of 31 species (including
one assumed native species, Rottboellia cochinchinensis) that emerged as the highest
priorities for control within the collective areas covered by the PMPs. These are set
out in Figure 1.
It is important to note that the outcome of DNR exercise is quite different from that
which is required from the current exercise. Inspection of Figure 1 will reveal that
application of the MODSS incorporated considerations other than invasive risk. While
this was accommodated within the first of two main discrimination components (ie,
impact and research), other factors such as economic and socio-cultural impacts
were also included, along with various factors associated with research activities,
against which the species were ranked. Of relevance here is the fact that the species
that emerged as priority weeds for research are likely candidates for problematic
environmental weed standing since they have been identified by a range of individuals
reflecting a variety of interests throughout the region. Accordingly, those inclusions
formed the basis of the sample screened utilising the proposed Wet Tropics RAS (see
Section 5.2.5 below)
3.2
Once a pest plant has arrived in a new host environment both long-term environmental
and economic benefits can accrue from its early detection and control and/or
eradication. This prompts a need for a systematic assessment of large numbers of
species whose impact may not be evident now but which may be in early stages of
invasion.
Virtue et al. (in press) point out that qualitative differences exist between decision
support systems for preventing introductions of unwanted species and those concerning
selection of species for control management. They claim that quarantine decisions
proceed on the basis of predicted negative impacts and potential area over which
that impact may be sustained, while control prioritisation will involve similar
considerations plus others that are associated with ease of treatment and potential for
control success. In addition, if the focus is on management for biodiversity
conservation, other factors such as the particular suceptibility of constituent native
species, assemblages and functionally significant landscape features such as
waterways and wetlands, needs to be accommodated.
The 10 local government areas comprise Atherton Shire, Cairns City, Cardwell Shire, Cook Shire, Douglas Shire,
Eacham Shire, Herberton Shire, Hinchinbrook Shire, Johnstone Shire and Mareeba Shire. Thuringowa City takes in
part of the southernmost protion of the bioregion but is largely marginal and not considered here.
Page 19
Page 20
3.2.1
Significance of Impact
Current Level of Impact
1. Distribution relative to disturbance regime
a. found only within sites disturbed within the last 3 years
b. found in sites disturbed within the last 10 years
c. found in mid-successional sites disturbed 11-50 years before present (BP)
d. found in late-successional sites disturbed 51-100 years BP
e. found in high-quality natural areas with no major disturbance for 100 years
2. Abundance
a. number of populations (stands)
(1)
few; scattered (<5)
(2)
intermediate number; patchy (6-10)
(3)
several; widespread and dense (>10)
b. areal extent of populations
(1)
<5 ha
(2)
5-10 ha
(3)
11-50 ha
(4)
>50 ha
3. Effect on natural processes and character
a. plant species having little or no effect
b. delays establishment of native species in disturbed sites up to 10 years
c. long-term (more than 10 years) modification or retardation of succession 7
d. invades and modifies existing native communities
e. invades and replaces native communities
4. Significance of threat to park resources
a. threat to secondary resources negligible
b. threat to areas' secondary (successional) resources
c. endangerment to areas' secondary (successional) resources
d. threat to areas' primary resources
e. endangerment to areas' primary resources
5. Level of visual impact to an ecologist
a. little or no visual impact on landscape
b. minor visual impact on natural landscape
c. significant visual impact on natural landscape
d. major visual impact on natural landscape
Total Possible =
B. Innate Ability of Species to Become a Pest
1. Ability to complete reproductive cycle in area of concern
a. not observed to complete reproductive cycle
b. observed to complete reproductive cycle
-10
1
2
5
10
1
3
5
2
3
5
0
3
10
15
0
2
4
8
10
0
2
4
5
50
0
5
Page 21
2.
3.
4.
5.
6.
7.
8.
9.
Mode of reproduction
a. reproduces almost entirely by vegetative means
b. reproduces only by seeds
c. reproduces vegetatively and by seed
Vegetative reproduction
a. no vegetative reproduction
b. vegetative reproduction rate maintains population
c. vegetative reproduction rate results in moderate increase in population size
d. vegetative reproduction rate results in rapid increase in population size
Frequency of sexual reproduction for mature plant
a. almost never reproduces sexually in area
b. once every five or more years
c. every other year
d. one or more times a year
Number of seeds per plant
a. few (0-10)
b. moderate (11-1,000)
c. many-seeded (>1,000)
Dispersal ability
a. little potential for long-distance dispersal
b. great potential for long-distance dispersal
Germination requirements
a. requires open soil and disturbance to germinate
b. can germinate in vegetated areas but in a narrow range or in special conditions
c. can germinate in existing vegetation in a wide range of conditions
Competitive ability
a. poor competitor for limiting factors
b. moderately competitive for limiting factors
c. highly competitive for limiting factors
Known level of impact in natural areas
a. not known to cause impacts in any other natural area
b. known to cause impacts but in other habitats and different climate zones
c. known to cause low impact in natural areas in similar habitats and climate zones
d. known to cause moderate impact in similar habitats and climate zones
e. known to cause high impact in natural areas in similar habitats and climate zones
Total Possible =
3.2.2
1
3
5
0
1
3
5
0
1
3
5
1
3
5
0
5
0
3
5
0
3
5
0
1
3
5
10
50
Page 22
Box 2. WRAS question sheet commissioned by the Australian Weeds Committee & Plant Industries
Committee (Pheloung 1995)
Botanical Name: ..
Common Name:
Outcome: .
Score: .
Answer yes or no, or leave blank unless indicated. Scores for a question typically 1=yes, -1 or 0=no, 0=dont know.
The climate & weed elsewhere sections generate a score using a weighting system: a better climate match increases
the climate weight and a poorer quality match also increases the weight because of greater uncertainty and, therefore,
greater risk. Weed elsewhere responses are multiplied by the climate weight to generate the final score for each
question. (Note: A = agricultural, E = environmental, N = nuisance, C = combined.)
Biogeography/Historical
1. Domestication/Cultivation
2. Climate/Distribution
3. Weed Elsewhere
(A)
(C)
(C)
(C)
(C)
(C)
(N)
(A)
(E)
4. Undesirable traits
(A)
(C)
(C)
(A)
(C)
(C)
(N)
(E)
(E)
(E)
(E)
(E)
5. Plant type
5.01 Aquatic
5.02 Grass
5.03 Nitrogen fixing woody plant
5.04 Geophyte
(E)
(C)
(E)
(C)
6. Reproduction
(C)
(C)
(C)
(C)
(C)
(C)
(C)
7. Dispersal Mechanisms
(A)
(C)
(A)
(C)
(E)
(E)
(C)
(C)
8. Persistance attributes
Biology/Ecology
(C)
(A)
(A)
(A)
(E)
Page 23
3.2.3
I.
L.
M.
H.
I.
L.
M.
H.
I.
L.
M.
H.
I.
L.
M.
H.
Page 24
Impact ranking is achieved by scoring responses addressing parts A. and B. and at least one other part in this
section according to the following:
HIGH = H in A and B; H in A. or B. and M-H in at least one other category; M in A. and B. and H in at least one
other category.
MEDIUM = M in A. or B. and M-H in at least one other category; L in A. or B. and H in at least one other
category.
LOW = if species scores M in at least one other category.
INSIGNIFICANT = all other combination of ascriptions.
not aggressive has none of the above characteristics or only one or two to a very small extent
somewhat aggressive has one or two of the above to a small extent
aggressive has >2 of the above but only 1-2 to a great extent
extremely aggressive has 3 or more of the above characteristics to a great extent.
B.
Is the species known to be invasive beyond its native range in other areas? [list other areas]
C.
Page 25
L.
M.
H
5-20 areas
21-100 areas
> 100 areas
C. Extent of range that has been identified as problematic by land managers
I.
0-5%
L.
6-20%
M.
21-50%
H.
>50%
D. Potential cover of species in strata where it occurs
J.
infrequent (< 10%)
L.
fair coverage but < 50%
M.
dominant (50-90%)
H.
grows in monospecific stands (90-100%)
Impact ranking is achieved by scoring responses addressing part A. and at least two other parts in this
section according to the following:
HIGH = H in A and M-H in at least one other category; M in A. and H in at least one other category.
MEDIUM = H in A. and L-I in all other categories; M in A. and M in at least one other category; M in A. and L-I
in all other categories; L in A. but H in at least one other category
LOW = if species scores L in A. and M in at least one other category; if scores I in A but H in at least one other
category.
INSIGNIFICANT = all other combination of ascriptions.
While this system addresses a comparable issue to the task at hand, it presupposes a
considerable body of knowledge for any given taxon.
This necessitates an
understanding of both species biology and current distribution. Since control
feasibility is a secondary consideration to innate weediness, only sections I and II are
directly relevant to weed risk assessment per se.
3.2.4
Page 26
Box 4. Categories and ranking system of the Hawaiian WRAS (Teytaud 1998)
A.
1.0
1.5
2.0
2.5
3.0
3.5
4.0
C.
1.
2.
3.
4.
SCORING SYSTEM FOR USE WITH THE HEAR RISK ASSESSMENT MODEL (Note: leave categories
blank only if information is unavailable)
Score #1
HIGHEST Cronk & Fuller Invasive Category (for number codes, see above) presently
known for this species ELSEWHERE IN THE WORLD, based on information obtained from Cronk &
Fuller (1995) and/or other literature and/or experet opinion
Score #2
TOTAL NUMBER of different types of Cronk & Fuller Climate Zones presently known to be
occupied by this species ELSEWHERE IN THE WORLD, based on Cronk & Fuller, etc (as above)
Score #3
HIGHEST HEAR Invasive Category presently known for this species on the main Hawaiian
islands based on information from from the literature and/or expert opinion
Score #4
HIGHEST HEAR Negative Impact Category presently known for this species on the main
Hawaiian island based on information from from the literature and/or expert opinion
Score #5
TOTAL NUMBER of different types of HEAR Climate Zones within the environmental
envelope of the species in Hawaii, and presently/potentially invaded by this species on the main Hawaiian
islands calculated using information from the HEAR climate envelope GIS model
Page 27
Score #6
TOTAL LAND AREA (square miles) of HEAR Climate Zones within the environmental
envelope of the species in Hawaii, and presently/potentially invaded by this species on the main Hawaiian
islands calculated using information from the HEAR climate envelope GIS model
Score #7
TOTAL LAND AREA (square miles) of existing Natural/Semi-natural Physiognomic
Vegetation Types (ie, Ecoregional Sub-units or the equivalent to Regional Ecosystems in the Wet Tropics
Bioregion) calculated by intersecting the HEAR climate envelope GIS model with digital map of
Ecoregional Sub-units enter 0 if no such area is believed to be threatened
Score #8
TOTAL LAND AREA (square miles) of Managed Areas potentially invadable if this species
were to attain its potential distribution on the main Hawaiian islands calculated by intersecting the HEAR
climate envelope GIS model with digital map of Ecoregional Sub-units enter 0 if no such area is
believed to be threatened
Page 28
(4) shrubs or small trees that mostly spread by a combination of seeds and vegetative
means to form dense stands preventing other herbaceous or woody growth
(incidently, this group contains species of Leucaena, Lantana and Rubus that pose
similar problems to native communities of the Wet Tropics)
(5) trees that are invading slowly because they are in the early stages of expansion
and/or have heavy seeds that reduce their dispersal capability but which, because
of their size, will have dramatic impacts on lower growing native vegetation
(Mangifera indica, and to a lesser extent Persea americana, may be considered to
be natural members of this group within the Wet Tropics)
(6) trees that spread rapidy by small wind or animal (particularly bird) dispersed seeds
and which form dense stands (eg, in the Wet Tropics, Spathodea campanulata is
representative of the former sub-group and Psidium guajava of the latter), and
(7) a single herbaceous species the tomato (Lycopersicon esculentum) that is
having a unique environemental impact through hybridising with the native
L. cheesmanii and threatening its survival on some islands.
These groups are based on a subjective assessment of what is known of their invasions
and impacts and, in the absence of a formal RAS, can be further ranked in decreasing
order of importance as Group 6 > Group 5, Group 2 > Group 1, with some within each
group meriting higher ranking than others, and so forth. A more objective RAS would
permit more precise comparisons and relative ranking than is possible with this
approach. To this end, an alien plant RAS for Galapagos is currently being developed
based on quarantine screening protocols and a recently formulated system being
implemented in New Zealand (NZDC 1997). The latter, in particular, includes the
following components:
1.
2.
3.
4.
Initiatives currently underway to assist weed control in the Galapagos Islands can
inform the formulation of a Wet Tropics regional RAS. They include a comprehensive
review of pertinent factors (see parts 1-4 of Box 5). It is considered that factors
affecting ability to control a given alien species need not be included in the initial
phase of weed risk assessment to be applied regionally but, rather, are a secondary
consideration. It is first of all important to focus on (1) which species are having or
will have the greatest ecological impact and (2) to reveal which of those species that
are currently restricted, uncommon and/or relatively innocuous that are virtual time
bombs and capable of doing much more than using space (Tye in press:30).
Page 29
3.2.6
Page 30
Invasiveness based on an assessment of the biology of the weed and its life history (maximum
weighting 1)
impact characteristics (maximum weighting 1)
potential and current area of spread (maximum weighting 0.5: comprising (i) current distribution
maximum weighting 0.25, and (ii) potential distribution maximum weighting 0.5 )
current primary industry, environmental and socio-economic impacts (maximum weighting 0.75
comprising: (i) current cost of control for agriculture and forestry maximum weighting 0.25, (ii)
environmental index maximum weighting 0.25 [itself comprising species up to 0.0625; communities
up to 0.0625; Interim Biogeographic Regions of Australia regions up to 0.0625; and monoculture
up to 0.0625], and (iii) social index maximum weighting 0.25.
MAXIMUM SCORE = 3.25
3.2.7
low
SCOR
E
Note: seedlings include vegetative growth forms and those from spores.
don't know
2. What is the weed's tolerance to average weed management practices in the landscape?
very high
high
medium
low
don't know
2
1
0
?
SCOR
E
3
2
1
0
?
Page 31
high
med.-high
medium-low
low
don't know
(c) Water
(d) Wind
(a) Flying birds
(b) Other animals
2 common
2
2 common
common
common
occasional
1 occasional
1
1 occasional
occasional
unlikely
0 unlikely
0
0 unlikely
unlikely
don't know
? don't know
?
? don't know
don't know
5. How likely is long-distance dispersal (>100m) by human means?
(a) Deliberate spread
(b) Accidentally by
(c) contaminated
by people
people and vehicles
produce
2 common
2
2
common
common
1 occasional
1
1
occasional
occasional
0 unlikely
0
0
unlikely
unlikely
? don't know
?
?
don't know
don't know
IMPACTS
6. Does the weed reduce the establishment of desired plants?
>50% reduction
Total
(a+b+c)
SCOR
E
5 or 6
3 or 4
1 or 2
0
3
2
1
0
?
SCOR
E
3
2
1
0
?
SCOR
E
Total
(a+b+c+d)
2
1
0
?
6, 7, 8
3, 4, 5
1 or 2
0
Total
(a+b+c+d)
6, 7, 8
3, 4, 5
1 or 2
0
25-50% reduction
10-25% reduction
<10% reduction
none
medium
low
none
don't know
3
2
1
0
?
SCOR
E
4
3
2
1
0
?
SCOR
E
don't know
7. Does the weed reduce the quality of products or services obtained from the landscape?
high
2
1
0
?
SCOR
E
10-50% reduction
<10% reduction
none
don't know
7.Does the weed reduce the yield or amount of desired vegetation?
>50% reduction
Page 32
1
0
?
8. Does the weed restrict the physical movement of people, animals, vehicles, machinery
and/or water?
high
Weed infestations are impenetrable throughout the year, preventing the physical
movement of people, animals, vehicles, machinery and/or water.
medium
Weed infestations are rarely impenetrable, but slow the physical movement of
people, animals, vehicles, machinery and/or water throughout the year.
low
Weed infestations never impenetrable, but slow movement of people, animals,
vehicles, machinery and/or water at certain times of the year.
none
The weed has no effect on physical movement.
don't know
9. Does the weed affect the health of animals and/or people?
high
medium
low
SCOR
E
3
2
1
0
?
SCOR
E
The weed is highly toxic and frequently causes death and/or severe illness in
people, stock, and/or native animals.
The weed frequently causes significant physical injuries (due to spines or barbs)
and/or significant illness (chronic poisoning, strong allergies) in people, stock,
and/or native animals, occasionally resulting in death.
The weed occasionally causes slight physical injuries or mild illness in people,
stock, and/or native animals, with no lasting effects.
The weed does not affect the health of animals or people.
3
2
1
0
?
none
don't know
10. Does the weed have major, positive or negative effects on environmental health?
major
positive effect
1
major
negative effect
1
minor or no
effect
0
don't know
?
Total
>3
2 or 3
1
(a + b + c + d + e + f)
SCORE FOR 6.
3
2
1
11. What proportion of the area is suitable for the weed?
> 80%
The weed has a potential to spread to more than 80% of the Area
60-80%
The weed has a potential to spread to 60-80% of the Area
40-60%
The weed has a potential to spread to 40%-60% of the Area
20-40%
The weed has a potential to spread to 20%-40% of the Area
10-20%
The weed has a potential to spread to 10%-20% of the Area
5-10%
The weed has a potential to spread to 5% and 10% of the Area
<5%
The weed has a potential to spread to less than 5% of the Area
unsuited
The weed is not suited to growing in any part of the Area
don't know
0 or less
0
SCORE
10
8
6
4
2
1
0.5
0
?
Page 33
simply an aid to decision-making, it is best to group weeds with similar importance scores, with respect to different
land uses. Weeds could be grouped as follows:
Groupings for Weed Importance score :
1
401-1000
DECREASING
2
201-400
SIGNIFICANCE
3
101-200
4
50-100
5
26-50
6
0-25
Why multiply the invasiveness, impacts and potential distribution scores?
Multiplying gives a greater spread in scores than adding (ie. range from 0-1 000 compared to 0-30).
Multiplying is logical, as it recognises the interactions between the criteria. If the impacts of a weed can be
measured in dollars per hectare per year, the potential distribution is known in hectares, and the invasiveness
(ie. rate of spread) is measured in terms of the increase in hectares compared to the previous year:
Impact
Potential Distribution
Invasiveness
$ / hectares / year
hectares
hectares(current year) / hectares (previous year)
When multiplying, all of the hectare units cancel so that weed importance is measured in total dollars per year. In
multiplying the invasiveness, impacts and potential distribution criteria scores, we are mimicking the above
calculation, without having the actual dollar and hectare figures.
3.3
Some workers (eg, Swarbrick, in Binggeli et al. 1998:22) in the area express
considerable doubt as to whether invasiveness can be adequately predicted and claim
that, given the right set of circumstances, any plant can become a weed. Despite the
justifiable skepticism, it is important to formulate systems that can provide some
indication of weediness risk. Any potentially useful system must include a basic set of
elements against which potential or existing plant introductions can be assessed.
Three basic factors ie, species characteristics, disturbance regimes and environmental
factors - are critical considerations in weed assessment (Binggeli et al. 1998:2). In
addition there are various other aspects of the host environment (or extrinsic factors)
that require evaluation in any system designed to rank exotic plants according to risks
posed, especially in light of the conservation management obligations within the Wet
Tropics region. Moreover, the manner in which an exotic species is introduced to the
recipient land (Maillet & Lopez 2000:12) can, along with the basic attributes of the
plant, the ecological characteristics of the host environment and the extent of
disturbance, determine the nature and speed of invasion.
Clearly there are certain intrinsic biological traits predisposing species to potential
invasiveness (Goodwin et al. 1999:423). However, it has been demonstrated by
Maillet & Lopez (2000:23) that no set of characters is common to weedy exotic
species. The ideal weed, it is argued by Noble (1989:302), is a plastic perennial
which will germinate in a wide range of physical conditions, grow quickly, flower
early, is self-compatible (ie, not possessing a specialised pollination system), produces
many [persistent] seeds that disperse widely, reproduces vegetatively and is a good
competitor. Goodwin et al. (1999:423) note also that it is important for successful
invaders to possess seeds that can germinate without pretreatment (as in vernalisation)
and that there should be short intervals between large seed crops. Noble (1989:308)
goes on to argue that the perenniality of a plant is little evidence of its invasive
potential in stable environments. Moreover, species that have long-lived seed pools
may pose great problems for weed control/eradication but that is a separate issue from
the prediction of invasiveness itself. Patently, traits relating to a species reproductive
Page 34
and growth system, dispersal capability3 and competitive ability are valuable indicators
of potential invasiveness and should feature prominently in any effective RAS.
Competitive ability, however, is not easily established precisely without field trials
under a range of conditions and other experiments. It may be inferred from extensive
observations elsewhere, and it is more likely that aspects of a plants gross biology,
that includes observations on life form, growth, reproduction and dispersal, will be
better documented in the existing literature and, therefore, more readily accommodated
within a RAS. Consideration of intrinsic traits for use in the proposed Wet Tropics
RAS is included within Section 4.2 below.
Despite the enormity of the problem of weed invasion, it is evident that most exotic
species tend to remain associated with areas of gross human disturbance, whereas
only a few establish in stable, natural vegetation (Maillet & Lopez 2000:12).
However, these do indeed pose major threats. Noble (1989:309) stresses that it is the
invaded environment, as much as the properties of the invading species itself, that
determine invasion success. These are of particular pertinence in the HEAR system
(see Box 4 above), are included in the ESRS (Box 1) and the WWPRS (Box 3), and not
only relate to degrees of disturbance that predispose systems to invasion, but also relate
to the special conservation status of species and ecological communities. Specific host
environment or extrinsic factors are incorporated within the proposed Wet Tropics
RAS as set out in Section 4.3 below).
Weediness elsewhere is regarded widely as one of the best predictors of invasiveness.
Citing Reichards (1994) work, Binggeli et al. (1998:23) reinforce this determination
on the basis of a comparison of 235 invasive species with 114 other introdutions that
failed to establish and spread. They claim that at present, species known to be
invasive elsewhere in he world under similar climatic conditions is still the best
predictor of invasiveness. It is appropriate that, immediately subsequent to
establishing whether a species is indeed native or exotic (as is the case with some
agricultural weeds rather than alien species that are environmental weeds within
natural systems), the extent to which it or a related (congeneric) species has
demonstrated invasiveness elsewhere must be evaluated.
Noble (1989:310) comments that while short-distance dispersal will increase both the predictability and rate of invasion,
that absence of inherent long-distance dispersal capacity is not a hindrance to invasiveness since humans are the main
vector. In short, it seems that species with a high reproductive output (even if unsuccessful) in native habitat have high
invasive potential, with large flowering and fruiting effort being the first clue to a successful invader (Noble 1989:306).
Page 35
4.0
The basic requirement of this exercise is not to screen potential imports but to evaluate
species already present that currently or potentially constitute major environmental
weeds. This is to serve as a basis for allocation of limited area management resources
within (and presumably about) the Wet Tropics WHA. In fact, this exercise can be
considered analogous to the calibration/validation testing of the WRA system proposed
for import screening use (Pheloung 1995:8). Analagous also, albeit at a different scale,
is national assessment of weeds already present in Australia.
Just as two critical numeric scores are used by import screening authorities to reject,
further evaluate or accept proposed introductions, a similar approach to ranking exotic
species may allow the differentiation among highest priority, sleeper and relatively
benign weeds that can prompt control and/or eradication, careful monitoring and
minimal strategic control management actions, respectively. The fact that protected
area boundaries and especially those often irregular and discontinuous ones that
characterise the Wet Tropics WHA - are not recognised by plants (and most animals)
means that the evaluation was conducted on a bioregional basis rather than confining
attention strictly to the WHA itself. Also any RAS that will have explicit management
utility must be tailored to fit both the invader and the invadee: ie, the autecological
and life history attributes of the species as well as the biotic and abiotic attributes of
the ecosystems being protected (Ewell 1986:228).
In the proposed RAS it is appropriate to aim at consistency with other approaches and
to derive a system that is robust, simple to apply and transparent. Hence, there is good
reason for a useful system being highly derivative, drawing closely upon those
elements of RASs in use or under development elsewhere to benefit from earlier expert
opinion. Moreover, data now being gathered on a vast range of plant taxa in such
compendia as the Global Invasive Species Database (Fondation dEntreprise Total
2000 issg@auckland.ac.nz ), and others associated with tropical woody weeds (eg,
Binggeli et al. 1998), are compatible with such systems and therefore more amenable
for inclusion in any purpose-built RAS when screening species not known locally.
In an assessment of invasiveness there are two fundamental questions: (1) what are the
biological characteristics of an invasive species; and, (2) how does that allow us to
predict what species will be invasive? Biological traits including reproduction,
establishment, growth, dispersal, and competitive ability, genetic plasticity are know to
be fundamentally indicative of invasive potential (see Section 3.3). While there are
many gaps in detail, these are explicit, whereas impacts and extrinsic attributes of the
host environment are less so. Williams & West (2000:428) list a group of key
attributes of plants that indicate a potential for weediness in native ecosystems. These
are set out in Table 4.
As well as intrinsic (known biological attribute) factors there are extrinsic
(environmental, etc) factors that require consideration ie, critical landscape features
and species and communities at risk. Consideration is given below as to how such
attributes are employed within existing systems that are used to determine
environmental weed risk. It is, however, intended that more explicit understanding of
the peculiarities of the subject region and special aspects of its ecology and constitutent
communities and species be explicitly accommodated in the RAS.
Page 36
Table 4: Characteristics of plants that are indicative of a potential for weediness in natural
ecosystems (after Williams & West 2000:Table 3).
high input of viable propagules
short (<2 years) development time to reproductive maturity
seeds/other reproductive units with prolonged (>5 years) periods of dormancy/residency in seed bank
high rate of aerial or subterranean biomass production, particularly under conditions of low light, water
and/or nutrient availability
dense and spreading foliage/canopy
efficient long distance (>1 km) dispersal capaiblity
presence of interspecific allelopathic properties and/or absence of intraspecific allelopathic properties
successful coloniser of disturbed or bare ground
reproductive strategies that facilitate survival in fire-prone environments
broad distribution over a range of distinct climatic types
low suceptibility to attack by phytophagous organisms
4.1
With respect to woody weed invasion in the tropics, Goodland et al. (1998:8/2) argue
that every invasive event is unique and is affected by the species distinctive set of
attributes and specific local environmental factors and biological communities.
There are, however, certain characteristics that predispose plants for weedy behaviour.
In fact, these traits are often those for which plants have been introduced as robust
agricultural or ornamental adventives. Consideration of the most diagnostic of those
intrinsic traits is a fundamental requirement of any effective RAS.
In a major global review of woody invasive species in the tropics, Binggeli et al.
(1998:14-15) note that birds are the major dispersal agents of the most invasive weeds
and are implicated in the spread of 43% of those species considered. Wind dispersal is
of secondary significance, accounting for dispersal of 20% of those species. It is
appropriate, therefore, that dispersal mode and distance (along with some measure of
propagule production) be incorporated into the Wet Tropics RAS. Pointers to
invasiveness in tropical environments include (i) high habitat disturbance and broad
ecological amplitude; (ii) short generation time; (iii) high reproductive output; (iv) high
diffusivity (dispersal capability); and (v) high numbers of invading individuals
(Binggeli et al. 1998:22).
4.2
Page 37
Table 5: Treatment of intrinsic traits amongst the various risk assessment systems reviewed
Intrinsic Attribute
Specific Assessment
System
it/congener
elsewhere a
weed
known level of
life form
and/or niche
ESRS of US
Department of Interior impact in natural
areas, habitats,
National Parks Service climates
(Hiebert &
Stubbendieck 1993)
Australian WRA
protocols (Pheloung
1995)
climates in
distribution
introduction
history
extent naturalised
beyond native range
congeneric weed
type of weediness
exhibited
WWPRS of US Nature
Conservancy (Randall
et al., in press)
is species known
to be invasive
elsewhere?
invasive category
elsewhere
where invading
[habitat range]
Assessment to
determine WONS
(Thorp 1999)
Weed Assessment
Scoresheet of the SA
Animal/Plant Control
Commission (Virtue
2000)
4.3
existence of
undesirable traits
(eg, thorns, burrs)
plant type
(aquatic, grass,
geophyte, N-fixer)
climbing or
smothering growth
habit
reproductive
capacity and
mode
extent of
completion of
reproductive cycle
mode
extent of
vegetative reprod.
frequency of
sexual reprod.
No. of seeds per
plant
reproductive
success
seed production,
longevity &
viability
self-compatibility
reproduces by
vegetative
fragmentation
pollination
minimum
generative time
mode
seed production
seed viability
rate of spread
dispersal
mode and
capability
potential of long
distance dispersal
establishment needs
ditribution in
relation to
disturbance regime
germination
requirements
dispersal mode
(wind, water, bird
and/or intentional/
unintentional
human dispersal)
weed of disturbed
areas, agriculture or
environmental weed
tolerant of or
benefits from
mutilation and/or
cultivation
extent of local
proliferation
long distance
dispersal potential
extent to which it
establishes in
disturbed and.or
successional areas
dependence on
disturbance
life history
strategy
[habitat range]
reproduction
likelihood &
mode of longdistance dispersal
likelihood &
mode of humaninduced dispersal
dependence on
disturbance
Appreciation of the fact that invasiveness and risk is not only dictated by inherent alien
plant qualities but also by attributes of the host environment led also to an evaluation
on the extent to which these were utilised among the various screening/ranking
systems (Table 6). All systems reviewed included an assessment of impact or threat to
native communities (and generally to native species) or alluded to attributes such as
sociability (as in able to grow in monospecific stands) and/or allelopathy and toxicity.
Table 6: Treatment of extrinsic traits amongst the various risk assessment systems reviewed
Page 38
Extrinsic Attribute
Specific
Assessment System
distribution
ESRS of US
Department of
Interior National
Parks Service
(Hiebert &
Stubbendieck 1993)
Australian WRA
protocols
(Pheloung 1995)
spatial pattern of
infestation (ie,
widespread,
scattered)
areal extent
WWPRS of US
Nature
Conservancy
(Randall et al., in
press)
current range
(area)
No. of
infestations
abundance
environmental
tolerance
[incorporated in
distribution
attribute]
[related to
disturbance regimes
& successional
status]
climate match
environmental
[incorporated
partly in rate of
spread]
Weed Risk
Assessment in
Hawaii (Teytaud,
1998; Thomas, in
press)
Weed Risk
Assessment in the
Galapagos Islands
(Tye, in press)
Assessment to
determine WONS
(Thorp 1999)
[incoporated in
abilty to grow in
monospecific
stands]
current area of
spread
Weed Assessment
Scoresheet of the
SA Animal/Plant
Control
Commission
(Virtue 2000)
versatility
shade tolerance
grows on infertile
soils
competitive ability
includes tolerance of
a range of conditions
effect on native
communities
and/or species
threat to or
endangerment of park
resources
modification of
system succession or
ecosystem replacement
[related to system
successional
modification or
replacement]
creates a fire
hazard in natural
ecosystems
influence on
degree of
alteration of system
processes (eg, soil
nutrients, & water,
sedimentation rates,
fire-proneness)
community structure
potential cover of
species in strata where
it occurs (able to grow
in monospecific stands)
influence on
community
composition
conservation
status/significance of
community or species
at risk
[partly included in
known/suspected to
assessment of
cause replacement of
economic losses on
natural/semi-natural of
developed
high diversity, etc.
agricultural,
known/suspected to
housing, commercial pose significant threats
& industrial lands]
or extinction to native
floral or faunal
communities or species
with special
conservation status
habitat range
capability of
cause conspicuous or
potential area of
spread
[weighting imposed
proportional to bioregional significance
of species or
communities]
does weed prevent
establishment of
desired vegetation?
extent of reduction in
biodiversity so as make
area unsuitable for
nature conservation
toxicity to native
animals
effect on system
processes
drastic changes in
community
composition
has cryptic effects
(eg, trees in treeless
communities)
severely impacts on
native r&t species
known/suspected
to cause significant
alterations of
natural fire regimes
of native
communities,
energy flows,
materials or mineral
cycling, moisture
relationships or
other critical ecosystem processes
cause drastic
changes in habitat
structure (eg
tendency to form
monospecific
stands) by
suppressing recruitment or by allelopathy or changing
nutrient status
[possibly
incorporated in
previous attribute]
does weed have
effect on food,
shelter, fire regime,
nutrient levels, soil
salinity/erosion,
silting of waterways
or soil watertable?
Page 39
and that are, or can be, modified by invasion of exotic species. Clearly, this is a vital
component of an appropriate RAS against which invasive species can be ranked.
However, in the cases of exotic species that have yet to establish in the novel
environment, assessment depends upon the existence of information about their
occurrence in other places and ecosystem impacts that have occurred as a result.
Environmental tolerance, while interpretable as an intrinsic rather than extrinsic
attribute, can relate to properties of the host environment as well as to an exotic
species capacity to exploit those properties. Such attributes are indicative of plantenvironment interactions that reflect not only autecological aspects but also host
environment properties. In some instances this factor is included as a matching
exercise between the climates or landsystems of a plants native range and those of the
host environment. The HEAR system employs a sophisticated GIS matching of such
factors and similar comparative systems (eg, BIOCLIM/ANUCLIM, CLIMATE,
CLIMEX Kriticos & Randall in press) are either employed or under development in
Australia for the prediction of potential weed distributions that can be used to rank
species and to direct management efforts. In the interest of ease of application,
inclusion of this attribute in the proposed RAS is explicitly confined to assessment of
exotic aquatic plants as the versatility component, although it is, in part, associated
with the intrinsic attribute, competitive ability, in that part of the RAS applied to
terrestrial species.
Other factors that are again somewhat equivocally included in the extrinsic category
relate to properties of populations of exotic plants already present in a recipient
environment. Factors such as distribution and abundance, therefore, differentially
contribute to the assessment process and are dependent upon the stage of invasion of a
species. These attributes are occasionally employed in RASs but are more commonly
encountered in ranking schemes to inform weed management priorities. Despite this,
assessment of current distribution and abundance of existing weeds can reflect not only
stage of invasion but propensity to invade (and therefore point to risk) and can provide
a link between weed risk assessment and management.
4.4
Ranking Methodology
Page 40
ADD SCORES FOR STEPS 2 & THEN A3-A5 - MULTIPLY BY 2 TO PROVIDE A TOTAL SCORE OUT
OF 100
STEP 3B ASSESSMENT OF TERRESTRIAL (including SEMI-AQUATIC) TAXA
STEP 3 Gross invasiveness: What is the species ability to establish among existing plants?
very high seedlings readily establish within dense vegetation or amongst thick infestation of other weeds (score 5)
go to step 5
high seedlings readily establish within more open vegetation or amongst average infestations of other weeds
(score 4) go to step 5
medium seedlings mainly establish when there has been disturbance (tree clearing, mowing, temporary floods or
droughts) to existing vegetation (score 3) go to step 5
low seedlings mainly need bare ground to establish - eg, litter removal with cultivation, overgrazing, fire (score 2)
go to step 4
dont know (score 1) go to step 4
Note: seedlings include vegetative growth forms and, as in ferns, those from spores.
STEP 4 Does the species pose specific problems for native wildlife? NO STOP
Yes go to step 5
STEP 5 ASSESSMENT OF INTRINSIC (BIOLOGICAL) TRAITS
Tick the following checklist:
5.1 Reproduction:
! reproduces readily both vegetatively and by seed ! if reproduces by seed produces >1000 p.a.
! reproduces more than once per year ! rapid growth to reproductive maturity ! seeds remain viable for 2 years
! possesses rapidly spreading culms/stolons/rhizomes that may root at the nodes! resprouts readily when cut! other
5.2 Competitive ability: ! highly successful competitor for limited resources ! tolerates a wide range of
environmental conditions and/or is stress tolerant ! has ability to germinate in naturally vegetated areas under a wide
range of conditions
! is allelopathic ! lacks predators/control agents in its host environment! other
Page 41
5.3 Dispersal capability: ! rapid local proliferation of seeds ! adapted to long distance (eg, dispersed by birds;
has small water-borne or wind-borne seeds) ! other (eg, is adapted to medium distance dispersal by other animal
vectors)
ADD EACH TICK to give an accumulated score and rank accordingly:
extremely aggressive has 10 of the above traits and several ( 5) to a great extent score 15; go to step 6
very aggressive ie, has 5-9 of the above characteristics with 3 to a great extent score 10; go to step 6
potentially aggressive ie, has >3 of the above but only 1-2 to a great extent score 5; go to step 6
rarely aggressive ie, has 1-2 of the above to some extent score 2; go to step 6
relatively benign ie, has none of the above characteristics on only 1-2 to a very small extent score 1 STOP
STEP 6 ASSESSMENT OF EXTRINSIC (HOST ENVIRONMENT) FACTORS
6.1 Conservation status of communities/species at risk from invader
area at risk from invasion is highly significant ie contains 1 endangered Regional Ecosystem/species score 5
area at risk is significant ie, contains 1 of concern/vulnerable Regional Ecosystem/species score 4
area at risk is of moderate significance ie, may contain endemic species/good representative ecosystems score 3
area at risk contains communities of low significance eg common/widespread habitats, no r&t species score 2
conservation status of area insignificant ie, extent of human impact considerable, native species residual score 1.
6.2 Ability to disrupt native ecosystem function
major, possibly irreversible alteration/disruption of ecosystem processes (eg, fire-sensitive system more fire-prone,
chokes drainage channels, fixes nitrogen in oligotrophic system, drains wetland) score 5
significant alteration of system processes (eg, increases sedimentation rates, reduces open water habitat, shades
canopy, understorey and/or groundcover) score 3
some influence on ecosystem properties (eg, a perceivable but mild influence on soil nutrients) score 1
no perceivable impact on ecosystems processes/impact unknown score 0
6.3 Ability to disrupt ecosystem structure
major alteration of structure ie, covers canopy, forms monospecific stands eradicating most layers score 5
significant impact on one or more strata creates new layer or eliminates an existing stratum - score 4
significantly invades/replaces a single stratum - eg invades/eliminates groundcover or understorey score 3
influences structure in one stratum eg, changes density within a layer score 2
no structural impact establishes in existing stratum without altering stratification/density greatly score 1
6.4 Ability to disrupt native ecosystem composition
causes major alteration in floristics ie, results in extirpation of one or more native species, reduces native
biodiversity or facilitates increased exotic species representation score 5
significantly alters community composition ie, produces a significant population reduction in one or more native
species by displacement score 4
produces some influence on floristic composition reduces one or more native species population by reducing
recruitment score 3
little perceivable impact on native populations score 1
6.5 Current abundance in area
large populations with extensive (>20% of region) distributions score 5
large populations with widespread (10-20% of region) distributions score 4
moderate populations with relatively restricted and/or patchy distributions score 3
small populations with few significant infestations score 2
small populations with limited and/or very sparse distributions score 1
ADD SCORES FOR STEPS 2-3 & 5-6, MULTIPLY BY 2 TO PROVIDE A TOTAL SCORE OUT OF 100
The primacy of the weed elsewhere attribute is clearly acknowledged by Reichard (in
press). Similarly, Rejmnek (in press) argues the importance of a species or a congener
of a species having demonstrated weediness in similar environments and that this
knowledge is very powerful in predicting invasive potential. Accordingly,
immediately after the initial screening step to dispense with native species, a ranking
was given to taxa that have exhibited weedy tendencies elsewhere (and to what extent)
or have congeners that are known weeds.
Champion & Clayton (in press:192) argue clearly for the basic distinction between
obligate aquatic and terrestrial species, especially given that many of the attributes
scored in general RAS models are not relevant to aquatic plant assessment, and provide
a risk assessment model specifically designed for the former. Hence, once preliminary
screening was conducted to determine exotic status and whether a species or its
congener(s) exhibited weediness, the aquatics and terrestrials (including some
emergent wetland species of non-obligate hydrophytes) were dealt with separately.
Page 42
The relative importance of each attributes contribution to overall risk is not well
understood. Therefore each is regarded as basically equivalent in the ranking system.
The rationale here is that relative weightings introduce greater measures of subjectivity
into the system and, thus, were avoided/underplayed. Thereafter the system regards
each component attribute as generally equivalent but incorporates an ordinal measure
of relative significance using staged scores (eg, extremely aggressive score 15; very
aggressive 10; potentially aggressive 5, and so forth) within a specified range.
With regard to extrinsic factors, it may be argued that one attribute, eg, ability to
disrupt ecosystem function or relative significance of the conservation status (ie,
endangered, vulnerable/of concern) of communities and/or species at risk, is of
higher significance than others. In the absence of any accepted means to differentiate,
each was scored iteratively to contribute to a final score.
Assessment of conservation status allowing invasion risk to be scored according to
communities and/or species at risk from the alien invader ie, endangered versus of
concern in the case of Regional Ecosystems (REs) or endangered and vulnerable in
the case of species, were drawn from official lists. These are Goosem et al. (1999) for
communities (REs) as in the Vegetation Management Act (1999) or according to
Wildlife Schedules of the Nature Conservation Act (1994) for species (also listed in
Goosem et al. 1999).
There was a certain dilemma regarding the inclusion of attribute 6.5 ie, current
abundance (Table 7) since this normally is associated with control feasibility than
risk per se. In this case, however, it served as a measure of host environment
susceptibility to date to this invader and a useful extrinsic criterion to score against.
The omission of economic impact, management costs and similar socio-economic
criteria that are often incorporated into other weed screening systems (eg, Randall et al.
in press, Tye in press, Virtue 2000) was intentional. Intuitively, these are secondary
considerations to inherent invasiveness potential and more appropriately considered
subsequently to environmental risk per se in order to prioritise weed species for
management action. Moreover, this is the approach generally employed to rank
agricultural pests where monetary values of crop production and pest control are more
tangible rather than in assessing environmental weeds.
The extent to which the proposed RAS provides a sensitive indication of
environmental weed risk now requires evaluation. Consequently, it is intended to
screen a sample of exotic species that have naturalised within the bioregion as a first
step in this evaluation process. Relative rankings can then be considered in
comparison with existing lists of prioritised invasive species such as those identified as
the worlds worst species (Fondation dEntreprise Total 2000), species classified as
WONS and the results from the application of other similar weed classification
systems. Furthermore, it is intended that eventually all naturalised species within the
Wet Tropics Bioregion will be processed using this system so that a greater number of
comparative rankings can be evaluated. It is also suggested that the proposed system
be circulated for expert comment in order that any deficiencies can be identified and
remedied prior to its wider application.
Page 43
5.0
Current assessment of weeds within the Wet Tropics Bioregion and the extensive
portion of that bioregion that comprises the Wet Tropics World Heritage Area was
based initially on the provision of a list of naturalised exotics from the EPAs WildNet
database. This was subsequently revised and replaced with a list based on
interrogation of the HERBRECS herbarium records database. The list contained
508 taxa comprising 475 species. Subsequently, 29 other exotics known locally to have
naturalised were included, resulting in a total of 504 species (Appendix 2)
Taxonomic nomenclatural changes are ongoing and frequently confound
comprehensive listing and assessment of plants. While it is not proposed to include
nomenclatural authorities with those taxa examined, an attempt has been made to
incorporate the most up-to-date taxonomic revisions and nomenclatural changes. This
process has been assisted greatly by B. Waterhouse (pers. comm.). Nomenclatural
changes include Wedelia trilobata to Sphagneticola trilobata, Duranta repens to
D. erecta; Praxelis clematidea is known now as Eupatorium catarium and E. riparium
is replaced by Ageratina riparia; Hiptage madablota is also no longer current and has
been superceded by H. benghalensis. Since the Queensland Herbarium is yet to
endorse the shift of genus to Urochloa (Waterhouse, pers. comm.), Par Grass will
continue to be referred to as Brachiaria mutica pending taxonomic reconsideration.
5.1.1 Additional Inclusions
Other species known locally to be naturalised, but due to lag time for processing
specimens and/or lack of collection, were not included on the official list have been
added to the list of taxa to be evaluated (Appendix 2). This process was based on the
authors knowledge of species occurrences within the region and was assisted greatly
by the extensive knowledge of exotic species possessed by colleagues (especially
B. Waterhouse of AQIS, D. Boorman and A. Small). Species not officially noted as
naturalised within the bioregion but included for risk assessment are listed in Table 8.
Several are regarded as doubtfully naturalised by the Queensland Herbarium.
5.1.2 Exclusions
No attempt was made to evaluate those infra-specific taxa that were included on the
official list of naturalised exotics. This somewhat masks important genotypic
differences that may have a bearing on invasiveness; however, due to resource
limitations it was not considered appropriate to differentiate.
Such exclusions include, for example, the three varieties of Mimosa pudica, and
similarly those for Emilia sonchifolia and others, that have been treated as a single
taxon. In addition, M. invisa is synonymous with M. diplotricha, and therefore is
excluded from the evaluation, and so forth.
Concatenation of infraspecifics reduces the original list of 508 taxa to 475 (including
hybrids). With the addition of the 29 species known locally to have naturalised but not
officially recorded (Table 8), a grand total of 504 exotics require evaluation using the
RAS (see Appendix 2). It should be recognised, however, that this total is almost
certainly an underestimate and the list should be reviewed regularly to remain current.
Page 44
Table 8: Additional taxa known to have naturalised within the Wet Tropics Bioregion but not
recorded in official (Queensland Herbarium) list of naturalised exotics.
FAMILY
SPECIES
Common Name
Origin
ACANTHACEAE
Barleria rosea
ANACARDIACEAE
Schinus terebinthifolia
Pepper Tree
Central America
APOCYNACEAE
Cascabela thevetia
South America
ARACEAE
ARECACEAE
Yelow Oleander,
Captain Cook Tree
Golden Devils Ivy
Queen Palm
Trop. America
ASTERACEAE
Mikania micrantha
Mile-a-minute
Trop. America
COMMENLINACEAE
Zebrina pendula
CUCURBITACEAE
FABACEAE
Momordica charantia
Inga sp.
Balsam Pear
Icecream Bean
(palaeotropics)
Trop. America
FABACEAE
Macroptilium atropurpureum
Siratro
Trop. America
HYDROCHARITACEAE
Elodea canadensis
Pondweed
North America
MARANTACEAE
Thaumatococcus daniellii
Tropical (West)
Africa
MELIACEAE
MELIACEAE
MIMOSACEAE
Azadirachta indica
Chukrasia velutina
Acacia nilotica
Neem Tree
Mahogany
Prickly Acacia
India
Indo-malaysia
Tropical Africa
MORACEAE
Artocarpus ?communis
Jackfruit
Indo-malaysia
MYRSINACEAE
MYRTACEAE
Gramachama Cherry
Trop. America
MYRTACEAE
Eugenia uniflora
Brazil Cherry
Trop. America
PINACEAE
Pinus caribaea
Caribaean Pine
Trop. America
POACEAE
POACEAE
Andropogon gayanus
Hymenachne amplexicaulis
Gamba Grass
Hymenachne
Tropical Africa
Trop. America
POACEAE
Saccharum spontaneum
Wild Cane
Indo-malaysia
POACEAE
Sporobolus pyramidalis
Giant Rats-tail
Africa
POLYGONACEAE
Triplaris surinamensis
and/or T. americana
Ant Tree
South America
RUBIACEAE
Coffea liberica
Tree Coffee
Tropical Africa
RUBIACEAE
Musenda frondosa
SAPINDACEAE
Blighia sapida
Akee
Tropical Africa
SAPOTACEAE
Chysophyllum cainito
Star Apple
South America
South-east Asia?
South-east Asia
Central America
South Asia?
Tropical Africa
Comments
noted naturalising in Cairns
area from ornamental roadside
plantings (Boorman pers.
comm.)
infestations about the Wild
River, Herberton
syn. Thevetia peruviana
patchy infestations known
garden escapee establishing
along creeks
invasive along Priors Ck and
about Atherton
one of worlds worst weeds
infestations in Mission Beach
area treated
garden escapee establishing as
groundcover in forested gullies
widespread weedy vine
escapee from cultivation
introduced as food plant
widespread introduced pasture
legume
second record only for Qld
from Mazlin Ck, Atherton
(Werren , unpub. data)
natural sweetener; - showing
signs of invasion of
Whyanbeel area (Stanton pers.
comm.)
invasive in drier areas
escapee from plantations
WONS - as above (noted by
Boorman, pers. comm.)
noted in area by Boorman
(pes. comm.)
invading about Cairns City
(Boorman, pers. comm.)
Stanton (unpub.) notes this
food plant as naturalising
naturalising in various places
(see Werren 1998)
widely planted timber tree
spreading from plantations
introduced pasture grass
ponded pasture species now
a WONS
noted doubtfully naturalised
by Qld Herbarium
recorded on Tableland by
Sullivan (Little pers. comm.)
naturalising in Bramston
Beach area noted in Cairns
CC PMP
spreading in Daintree area
(Boorman, pers. comm.)
noted by Herbarium as
doubtfully naturalised
(Guymer pers. comm.)
naturalising in Bramston
Beach area (Jensen, pers.
comm.)
spreading in forests along
footslopes of the McAlister
Range behind Palm Cove
(Small pers. comm.)
tropical fruit plant nvading
about Kamerunga (Stanton
pers. comm.)
Page 45
5.2
Earlier consideration of the extent of weeds in the bioregion (Humphries & Stanton
1992) resulted in a list of eight species that were viewed as current or potential major
environmental weeds. Swarbrick (1993a, 1993b, 1993c) focussed on five of those high
priority weeds in subsquent investigations of distributions, autecologies and control
treatments. While all eight were discovered invading native vegetation communities
without being assisted by gross disturbance, some appear more problematic than others
(eg, Pond Apple) and risks associated with some (eg, Clitoria laurifolia, Sanchezia
parvibracteata) seem, at least subjectively, to have been over-emphasised. This
constitutes a problem in the weed risk assessment field since different expert
approaches will apply different experiences and approaches to the same task. What is
required is a system that is less subjective, and while qualitative rather than
quantitative, can be applied by a range of individuals according to an agreed protocol.
A more recent exercise (Bebawi pers. comm.) has imposed some ranking of a subset of
the >500 introduced species known to have naturalised within the Wet Tropics region.
This has involved the ranking using a Multiple Objective Decision Support System
(MODSS) of the range of species addressed in ten Pest Management Plans (PMPs)
developed by the various local governments that span the bioregion (Table 9)
Table 9: List of the top 31 (30 exotics and 1 native species) Wet Tropics weeds that were
prioritised by MODSS. Species selection was based on the priority ratings given in the shires
and Cairns Citys Pest Management Plans (Bebawi pers. comm.).
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
Scientific name
Common name
Mikania micrantha
Chromolaena odorata
Mimosa diplotricha
Eupatorium catarium
Thunbergia spp.
Miconia calvescens
Annona glabra
Alternanthera philoxeroides
Hymenachne amplexicaulis
Andropogon gayanus
Cabomba caroliniana
Stachtarpheta spp.
Harungana madagascariensis
Senna obtusifolia
Elephantopus mollis
Cyperus aromaticus
Psidium guajava
Leucaena leucocephala
Brachiaria mutica
Spathodea campanulata
Hyptis spp.
Rottboellia cochinchinensis
Euphorbia heterophylla
Allamanda cathartica
Turbina corymbosa
Sphagneticola trilobata
Tithonia diversifolia
Sansevieria trifasciata
Eichhornia crassipes
Pistia stratiotes
Salvinia molesta
Mikania
Siam weed
Giant sensitive plant
Praxelis (syn. Praxelis clematidea)
Thunbergia
Miconia
Pond apple
Alligator weed
Hymenachne; Ponded pasture grass
Gamba grass
Cabomba
Snakeweed
Harungana
Sicklepod
Tobacco weed
Navua sedge
Guava
Leucaena
Para grass
African tulip tree
Knob weed; Stinking roger; Comb hyptis
Itch grass (Note: considered by most to be native)
Milk weed
Yellow allamanda vine
Turbine vine
Singapore daisy
Thithonia
Mother-in-laws tongue
Water hyacinth
Water lettuce
Salvinia
Page 46
Some of the more aggressive species that were deliberately introduced for stock forage
(except Hymenachne, Gamba Grass and Leucaena) are missing from this list (Table 7).
This is understandable since there has been a certain retiscence within local
government PMPs to consider useful (agricultural) plants especially pasture grasses
and legumes - that can also contitute major environmental weeds, either because of
policical (constituency) considerations and/or because of their ubiquity. However,
consideration of these within any comprehensive RAS is certainly warranted and it is
intended to supplement the test sample with examples of these taxa.
5.2.1 Natural groups of naturalised species based on habit/life
forms
The primary division of plants is into aquatic versus terrestrial categories. Champion
& Clayton (in press) argue for the distinctiveness of aquatic plants and for this primary
differentiation. Naturalised exotic aquatics within the region are set out in Table 10.
The seven aquatic macrophytes listed comprise three floating, two submerged and two
semi-emergent, species. Introduced ponded pasture species are essentially semiaquatic and will be considered within the larger group of terrestrial species. Emergent
semi-aquatic introduced species are also not included.
Table 10: Exotic aquatic macrophytes that have naturalised within the Wet Tropics region.
SPECIES
FAMILY
Common Name
Comments
Alternanthera philoxeroides
AMARANTHACEAE
Alligator weed
semi-emergent
Cabomba caroliniana
CABOMBACEAE
Cambomba
submerged a WONS
Eichhornia crassipes
PONTEDERIACEAE
Water hyacinth
floating
Elodea canadensis
HYDROCHARITACEAE
Pondweed
submerged
Pistia stratiotes
ARACEAE
Water lettuce
floating
ALISMATACEAE
Arrowhead
semi-emergent
Salvinia molesta
SALVINIACEAE
Salvinia
floating
The larger group of terrestrial plants can be further subdivided into natural groups
based on life form or habit. In a major review of tropical woody weeds, Binggeli et al.
(1998) have classified a provisional list of 235 invasive species into (1) trees > 15m
tall, (2) small trees 5-15m, (3) shrubs < 5m, (4) sub-shrubs (some parts somewhat
woody), and (5) vines. Non-woody species can be subdivided similarly into
meaningful groups such as herbs/forbs, graminoids and ferns.
More or less informal functional groups might be identified for the Wet Tropics in a
manner similar to those identified as indicative of different levels of risk and
invasiveness in the Galapagos (Tye in press:22-23). These comprise:
(i)
herbaceous/shrubby plants that are invading relatively slowly and whose main
effect is to dominate/replace the natural shrub/herb layer of more open
communities eg, Stachytarpheta spp., Hyptis spp.;
(ii)
Page 47
Gamba Grass, Molasses Grass and other introduced pasture grasses (note also
that these promote highly modified fire regimes);
(iii)
scramblers and climbers that have spread widely and, to some extent, have
become integrated into the natural communities the foremost of these being
Chromoleana odorata, Mikania micrantha, Turbina corymbosa, Thunbergia
spp., Sphagneticola trilobata and Solanum seaforthianum that have insidious
effects, while others such as exotic Passiflora spp., Mimosa diplotricha,
Momordica charantia and Allamanda cathartica exert at least intermittent
competition and can form dense mats to adversely affect the growth of a range of
native species;
(iv)
shrubs and small trees that form dense stands preventing other herbaceous or
woody growth eg, Leucaena leucocephala, Lantana camara, Miconia
calvescens and Murraya paniculata cv exotica (in the case of Leucanea and
Lantana, invasion can also cause major modifications to the natural fire regime);
(v)
trees that are invading slowly and/or more insidiously because they are sleepers
in the early stages of invasion or are more cryptic/less conspicous eg,
Parmentiera aculeata, Mangifera indica, Flacourtia jangomas, Blighia sapida that, while most have not yet necessarily caused serious ecological damage, pose
major threats by virtue of their size, or in the case of some such as Cucumber
Tree, can form dense monospecific stands displacing native species;
(vi)
trees which spread rapidly by small wind-borne or animal (particularly bird see
Wilkinson 1999) dispersal and which can form dense stands eg, Pond Apple,
Spathodea campanulata, Castilla elastica, Pinus caribaea, Psidium guajava and
Harungana madagascariensis that may have already established over wide
areas and threaten to displace native communities; and
(vii)
Plants can also be grouped into taxonomically related groups that may also have
consistent morphological/physiological expression. These groups may also share
attributes that confer a measure of invasiveness. Grasses ie, the family Poaceae
are one such group. During development of the AQIS system, expert comments such
as grasses should not be grouped together as guilty of weediness by association
(Pheloung 1995:16) were contributed. Some criticism of this approach was also
apparent during course of the weed risk assessment workshop held in Adelaide during
1999 (see Virtue in press). This was noted but not generally accepted because of the
comparative reliability as an indicator of risk given the large proportion of weedy
species within this natural group.
It is assumed here that this conclusion will apply to the large number of Wet Tropics
plant introductions. For instance, African C4 grasses have been implicated in
significant and often debilitating changes to the natural fire regimes of host
environments (Baker 1986, Vitousek 1986, Mooney & Drake 1989, Macdonald et al.
1989, Smith 1989). Wallmer (1994) has documented the high flammability of
Molasses Grass (Melinus minutiflora) and, to a slightly lesser extent, Guinea Grass
within this region. It is likely that a host of other related exotic grass species will
produce similar modifications to natural fire regimes.
Page 48
It is apparent from quarantine risk surveys (Williams et al. in press) that particular
locations furnish disproportionate numbers of invasive species. Williams & West
(2000:427) note that since the onset of European settlement there has been a gradual
shift over time in the countries of origin of most Australian weeds. Initially, European
countries were major sources and reflected the cultural biases and the need to be
surrounded by familiar plants and animals from the mother countries that was
enshrined in institutions such as acclimatisation societies. More recently, weeds of
American origin predominate in Queensland and, in Australia as a whole, Africa and
the Americas are the source continents of plants naturalised over the past three decades
(Williams & West 2000:427).
One of the reasons for undertaking the current exercise is that the Wet Tropics is rather
anomalous when compared with the rest of Australia and the RASs developed in other
parts of the country are unlikely to be directly applicable here. Correspondingly, the
origins of invasive species within this region are also likely to be different when
compared to those characterising other parts of Australia - particularly temperate
south-east regions. While some species with temperate origins will flourish on the
regions cooler Tablelands, and expansive dry country ones along the drier western
fringes of the bioregion combined with tropical stock forage grasses and legumes
Page 49
throughout, more exotic ornamental garden escapees are likely to be candidates for
environmental weed classification. These can come from a range of different
continents that impinge on tropical latitudes, particularly tropical America, Asia and
Africa. For example, of the 29 additional plant species known to have naturalised
regionally but not recorded on the Herbariums list (Table 6), 13 (45%) are from
tropical (ie, Central and South) America and seven (24%) each from Indo-Malaysia
(extending from India to South-East Asia) and tropical Africa. None are from
traditional sources such as Europe (including the Mediterranean) and western Asia.
5.2.3
Alligator Weed
Cambomba
Weed
elsewhere
5
5
Reprod.
mode
2
2
Nos of
reprod
organs
3
3
Dispers.
capacity
3
6
Versatility
7
7
Eichhornia crassipes
Water Hyacinth
Elodea canadensis
Pondweed
Pistia stratiotes
Water Lettuce
Arrowhead
Salvinia molesta
Salvinia
SPECIES
Common
Name
Alternanthera philoxeroides
Cabomba caroliniana
8
8
Score
(%)
56
62
10
74
64
68
64
66
Damage
For the terrestrial (including semi-aquatic) species, it was proposed initially to rank
every tenth taxon (ie, a 10% sample) on the emended list. In consultation with the
Senior Principal Scientist of the Wet Tropics Management Authority, a revised
approach was determined. It was agreed that a useful sample of taxa to trial a pilot run
of the scheme would be those identified by DNR as the 31 taxa (excluding the
aquatics) drawn from regional shire-based Pest Management Plans rated as highest
priorities for weed research (Table 9). These taxa were supplemented to a maximum
of 50 taxa with additional species drawn from the emended list of naturalised aliens to
represent other better known species from some apparently underrepresented groups
(eg, the single weedy palm tree, fruit plants and other ornamentals). The sample
assessed with the proposed Wet Tropics RAS is set out in Table 12.
Page 50
Habit4
Step
1
Step
2
Step
3
stop
special
Step
4
5.3
10
15
10
15
10
15
10
10
15
10
Score
5
6.5
12
18
14
11
12
18
17
15
14
13
16
13
11
10
10
21
18
14
19
Score
6
42
68
50
46
62
70
82
62
74
58
38
82
64
38
44
50
38
90
64
48
76
Total
X 2 (%)
Table12: Sample of terrestrial species, sensu lato, assessed using the RAS specifically developed for the Wet Tropics region.
9. Ageratina riparia
8. Aristolochia ringens
7. Syagrus romanzoffiana
6. Syngonium podophyllum
5. Allamanda cathartica
4. Annona glabra
3. Mangifera indica
2. Sansevieria trifasciata
1. Thunbergia spp.
Bignoniaceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Aristolochiaceae
Arecaceae
Araceae
Apocynaceae
Annonaceae
Anacardiaceae
Agavaceae
Acanthaceae
ButterflyTree
African Tulip
Cucumber Tree
Singapore Daisy
Japanese Sunflower
Mile-a-minute
Praxelis
Tobacco Weed
Siam Weed
Mother-in-laws Tongue
laurel vines
Ss
Ss
Tt
TT
TT
SS
stop
Cucurbitaceae
Convolvulaceae
Capparaceae
Caesalpiniaceae
Caesalpiniaceae
Spiderweed
Yellow Allamanda
Sicklepod
6.4
10
4
Balsam Pear
Turbine Vine
6.3
TT
TT
40
6.2
6.1
5.2
Pond Apple
Mango
TT
5.1
Queen Palm
SS
Common name
Dutchman's Pipe
SS
10
Family
Mistflower
Species
Bluetop
Ss
Cyperaceae
Navua Sedge
Page 51
Codes used to specify life-forms/habits are as follows: TT = large tree; Tt = small tree/tall shrub; SS = often tall woody shrub; Ss = subshrub and/or non-woody shrub; H = herb (including fleshy herbs
and graminoids); and, V = vine (including some very scandent shrubs).
Ss
Habit4
Step
1
Step
2
Step
3
stop
stop
Step
4
5.3
2
stop
10
Score
5
6.5
11
12
Score
6
12
46
56
18
Total
X 2 (%)
Milkweed
V
Verbenaceae
Verbenceae
Tiliaceae
Solanaceae
Selaginellaceae
Sapindaceae
Rutaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Passifloraceae
Myrtaceae
Myrtaceae
Mimosaceae
Mimosaceae
Meliaceae
Melastomataceae
Lauraceae
snakeweeds
Golden Dewdrops
Tree Strawberry
Brazilian Nightshade
Peacock Fern
Balloon Vine
Mock Orange
Itch Grass
Guinea Grass
Hymenachne
Par Grass
Gamba Grass
Stinking Passionfruit
Guava
Brazil Cherry
Leucaena
Neem Tree
Miconia
Avocado
Ss
SS
Tt
SS
Tt
SS
Ss
Tt
Tt
Tt
TT
stop
stop
10
10
2
stop
-
10
10
10
10
15
10
15
10
13
11
20
22
21
18
20
11
20
11
15
54
48
40
60
20
40
72
80
74
64
40
78
34
44
88
58
80
16
6.4
Butterfly Pea
1
3
6.3
Euphorbiaceae
Siratro
6.2
Fabaceae
6.1
5.2
Harungana
H
Ss
5.1
knob weeds
Common name
Lamiaceae
Family
Species
1
stop
1
stop
15
Page 52
5.3
It was decided at the outset to consider aquatic plants separately from the terrestrial
species utilising a different RAS. All seven exotic aquatic macrophytes known to
have naturalised within the Wet Tropics region are weeds elsewhere and therefore
receive the maximum score for this criterion of the RAS. Each differs slightly in
relation to other criteria and although the range of resulting scores (56-74 - Table 11)
is not nearly as large as for the terrestrial (including some wetland) species, there is
some indication that Water Hyacinth poses the greatest risk followed by the other two
floating aquatics, Water Lettuce and Salvinia. The submerged species rank
intermediately with the semi-emergent Alligator Weed ranking lowest. It is notable,
however, that all scores exceed 50 which is, in the case of the terrestrial species, a
high score indicative of significant environmental risk. Regionally, however, this risk
posed may not be as serious when compared with that in other regions owing to the
reliable Wet Season flood flows that normally flush the stream systems of the floating
aquatics and scour the semi-emergent and submerged ones.
5.4
Those 11 species from the sample with the highest scores (ie, _ 70) from an
environmental weed viewpoint, are those posing the greatest risks to natural systems
of the Wet Tropics Bioregion. These are, in decreasing order of assessed risk, Pond
Apple, Leucaena, Siam Weed, Singapore Daisy, Miconia, Hymenachne, Guava,
Thunbergia spp., Mikania, Par Grass, Guinea Grass and Cucumber Tree. The top
risk cohort includes two weeds that have been rated as of national significance
(Section 5.5 below). All have exhibited extremely aggressive weedy tendencies
elsewhere and/or are currently extremely aggressive weeds of the region, and, in the
case of Hymenachne, Par Grass and Guinea Grass, are very aggressive and greatly
impair ecosystem function. Arguably, these are clearly transformer species (sensu
Richardson et al. 2000:102) ie, invasive species that can change the character,
condition, form or nature of a natural ecosystem over a substantial area.
Several of these are also included a list of the worlds 100 worst alien invaders
(Fondation dEntreprise Total 2000) that includes 32 terrestrial plant species5. These
are Siam Weed (ranked 23rd), Leucaena (ranked 45th), Miconia (ranked 52nd), Mikania
(ranked 54th) and Singapore Daisy (which ranked 100th). Moreover, two of these
species were included on a highest-priority quarantine risk target list compiled by
AQIS (Waterhouse & Mitchell 1998) either prior to their entry to Australia as in the
case of Mikania, or because of the serious risk of reintroduction of Siam Weed. In the
latter case, its relatively restricted infestations were targetted by an eradication
program and, assuming the possibility of eradication, quarantine weed status was
required to ensure vigilence against its re-entry (Waterhouse pers. comm.).
The prevalence of purposefully introduced stock fodder species in the highest scoring
risk cohort is alarming, particularly in view of the continued promotion of Leucana by
primary industry support agencies and the continued cultivation and distribution of
seeds of Par Grass and Guinea Grass within the region. Prior to its elevation to
WONS status in 2000, Hymenachne was also promoted for use as a ponded pasture
species and was cultivated for distribution of its seeds.
5
The list of the worlds 100 worst invasive species comprises 32 land plants, 4 aquatic plants, 8 species of
micororganism (eg, banana buncy top virus), 26 invertebrate species, 8 fishes, 3 amphibians, 2 reptiles, 3 bird species
and 14 mammals (Fondation dEntreprise Total 2000).
Page 53
Those species that ranked with scores between 60-69 comprise Turbina corymbosa,
Parmentiera aculeata, Mangifera indica, Ageratina riparia, Andropogon gayanus,
Tithonia diversifolia, Spathodea campanulata and Solanum seaforthianum. Some
have demonstrated aggressive invasive properties elsewhere (eg, Mango, Gamba
Grass and African Tulip Noble 1989, Binggeli et al.2000), all but Cucumber Tree,
and to a lesser extent, Turbine Vine, are relatively widespread, and all have
demonstrated a high measure of invasiveness in relatively intact forest systems of the
region. The use of fruit from Cucumber Tree and Mango, as well as the widespread
dispersal of at least the latter by cassowaries (Casuarius casuarius johnsonii), fruitbats (Pteropus spp.) and Feral Pigs (Sus scrofa), accounts for its very extensive
distribution within moderately intact forests of the region. Ecologically, this
constitutes factor reinforcement that often sees mutually advantageous interaction of
alien species in this case, a plant and animal (Vitousek 1986:172). The ornamental
African Tulip and Brazilian Nightshade also possess well-developed long distance
dispersal capabilities (wind and bird dispersed seeds respectively) and are already
greatly invasive of intact native communities.
Taxa that ranked in the next score cohort (ie, 50-59) include Eupatorium catarium,
Azadirachta indica, Harungana madagascariensis, Stachytarpheta spp., Syngonium
podophyllum and Senna obtusifolia. This group corresponds to either widespread
invasive species of disturbed forest (as in the case of Praxelis, Snakeweed and
Sicklepod) or to invasive species occurring over a moderately limited area (eg,
Mistflower, Neem Tree, Harungana, S. podophyllum). Since Groves (1999:635)
argues that sleeper weeds fall somewhere between those recent incursions with a
high invasive potential known from their behaviour in other regions and the species
that have already become weeds of national significance, it is likely that these, and
some others in the previous group (ie, scores 60-69), are such.
Those species scoring between 40-49 include Sansevieria trifasciata, Duranta erecta,
Bauhinia monandra, Hyptis spp., Syagrus romanzoffiana, Mimosa diplotricha,
Momordica charantia, Cyperus aromaticus, Passiflora foetida, Murraya paniculata
cv exotica and Mutingia calabura. Several of these species exhibit invasiveness in
comparatively limited areas within the region and may be considered sleeper weeds;
while others (eg, the sedge, Hyptis spp., M. diplotricha, Balsam Pear6 and the
passionfruit) occur over more extensive areas where it is likely that disturbance has
enhanced their proliferation advantaging their invasive potential. It is considered that
below the score of 50 obtained by screening taxa using the newly devised RAS, the
environmental risk appears to be less serious and/or less pervasive.
A small group of four species fell in the range of scores just below 40 to 34
whereupon there was a significant natural gap in the ranked distribution. These
comprise Allamanda cathartica, Aristolochia ringens, Elephantopis mollis and
Eugenia uniflora. This is a diverse group comprising two ornamentals (Allamanda
and Dutchmans Pipe), a predominantly agricultural weed (E. mollis) and the birddispersed fruiting shrub, Brazil Cherry that is known to be naturalising at various
locations (eg, Werren 1998). These, and many others awaiting assessment, may
warrant consideration as sleeper weeds (see 5.6 below).
6
It is important to note that Balsam Pear (Momordica charantia) is the favoured host of the Melon-fly (Batroceras
cucurbitae) that is a quarantine pest occasionally incurring in islands of the Torres Strait (Waterhouse pers. comm.).
Should this insect reach the Wet Tropics, infestations of Balsam Pear would almost certainly facilitate its invasion and
greatly reduce the likelihood of success of any eradication program such as that which was successfully mounted against
its congener the Papaya Fruit-fly (B. papayae) within the region. This observation may confer more importance on the
control of this exotic plant regionally.
Page 54
Those lowest ranked species (with scores 20) are, with the exception of the
Avocado (Persea americana), essentially exotic ruderals, annual garden escapees or
weeds of disturbed places (eg, Cleome aculeata, Macroptilium atropurpureum). The
native Rottboellia cochinchinensis, that is almost exclusively an agricultural weed of
canefields, scored zero. The risk of any of these becoming major environmental
weeds appears to be inconsequential. Conspicuous infestations may constitute
aesthetic problems and inhibit the presentation of World Heritage values but are
assessed as little more than that.
5.5
Maillez & Lopez-Garcia (2000:12-13) note that there is clearly a lag time between
introduction and commencement of invasion and that a minor weed today may
become a major one in the future. The term sleeper weeds is defined as those
invasive plants that have naturalised in a region but not yet increased their population
size exponentially (Groves 1999:632). These are species which, while currently not
considered problematic, may be in the early phases of an explosive invasion. Groves
(1999:632) considers that these sleepers comprise a numerically large subset of the
invasive biota of Australia and deserve enhanced attention from research scientists
and resource agencies. Rozefelds & MacKenzie (1999:581), in their review of the
history of weed invasion of Tasmania, conclude by stating the seed for the next wave
of weed invasions has, unfortunately, already been sown and that most of the
previously considered adventives, sparingly established species or species with
status uncertain (ie, comparable to doubtfully naturalised category currently used
by the Queensland Herbarium) will eventually become established as weeds.
Given their current status, many sleeper weeds are not readily identifiable within the
list of >500 naturalised exotics in the region without further scrutiny. These, if not
identified as major problems elsewhere, may be detected by careful evaluation of their
intrinsic biological traits, including their environmental versatility and by seeking a
match between native and host environments.
Of those species screened, several appear to conform to the definition of sleepers.
These comprise Syagrus romanzoffiana, Bauhinia monandra, Eugenia uniflora,
Murraya paniculata cv exotica, Muntingia calabura and Duranta erecta. Most have
not yet become widespread problems, although several are considered problems at
Page 55
particular localities, but since all but one have fleshy fruits that are bird-dispersed,
they are are likely to become so in the not too distant future.
It was previously noted that Allamanda cathartica, Aristolochia ringens, and
Elephantopis mollis may also belong to such a category. It is significant that Elephant
Weed and Yellow Allamanda are, along with Golden Dewdrops and Brazil Cherry,
already regarded as invasive in Micronesia (Space 2001).
While it is appropriate to await formal assessment, other species not assessed may be
considered to belong to such a category. These include the introduced South
American tree, Schinus terebinthifolia. This species exhibited a considerable lag time
before an explosive invasion of South Florida (Ewel 1986:220). It is also ranked 84th
in the list of the worlds 100 worst invasive species (Fondation dEntreprise Total
2000:6). Already causing concern in and about Herberton, this bird-dispersed plant
may constitute a sleeper at least in parts of the Wet Tropics region.
Another regionally naturalised alien plant species are noted to be amongst the worlds
most serious invasive species (Fondation dEntreprise Total 2000). This is Hiptage
benghalensis. It is also listed by Space (2001) as invasive in Pacific Island
ecosystems. A watching brief is required to ensure that this species does not become
a major problem here.
Similarly, 326 species, some of which are native Wet Tropics plants, are listed (Space
2001) as invasive in ecosystems of the Pacific Islands (ie, Micronesia, American
Samoa or Niue). Inspection of this list reveals species that are in the process of
naturalising within the Wet Tropics that may also constitute sleeper weeds. These
include those previously noted, along with Andropogon gayanus, Anredera cordifolia,
Argyreia nervosa, Azadirachta indica, Bauhinia monandra, Bidens pilosa,
Brillantasia lamium, Buddleja madagascariensis, Caesalpinia decapetala, Canna
indica, Cardiospermum halicacabum, Cascabella thevetia, Castilla elastica,
Cenchrus ciliaris, C. echinatus, Centrosema pubescens, Cinnamomum camphora,
Clitoria terneata, Coccinia grandis, Coffea arabica, Cyperus rotundus, Digitaria
ciliaris, Echinochloa polystachya, Epipremnum aureum, Hedychium coronarium,
Hyparrhenia rufa, Hypochaeris radicata, Hyptis capitata, H. pectinata, H.
suaveolens, Jatropha gossypifolia, Macroptilium atropurpureum, Melinus repens,
Mimosa diplotricha, M. pudica, Momordica charantia, Montanoa hibiscifolia,
Muntingia calabura, Neonotonia wightii, Odontonema tubaeforme, Paspalum
conjugatum, P. dilitatum, P. paniculatum, P. urvillei, Passiflora edulis, P. foetida,
P. laurifolia, P. quadrangularis, P. suberosa, Pennisetum purpureum, Pinus
caribaea, Psidium cattleianum, Rubus alceifolius, Samanea saman, Sanchezia
parvibrachteata, Sanseviera trifasciata, Senna alata, Senna obtusifolia, Solanum
mauritianum, S. seaforthianum, S. torvum, Sorghum halapense, Stylosanthes
guianensis, Syngonium podophyllum, Thunbergia alata (together with other known
invasives belonging to this genus), Tradescantia spathacea, Triumphetta rhomboidea
and Urena lobata. This list also includes references to a host of known weeds in the
Wet Tropics and also to species such as Rhodomyrtus tomentosa and to others (eg,
Piper auritum) that are known to occur within the region (Waterhouse pers. comm.)
but which have not yet naturalised.
While the extent to which the plant has naturalised is limited and essentially confined
to highly disturbed situations, the extensive ornamental plantings of Bixa orellana
may, in time, prove problematic. This is so because the species is included by
Binggeli et al. (1998:29) on a provisional list of small (5-15m) invasive tropical trees.
Page 56
6.0
While factors explicit to management priority ranking (such as feasibility and cost of
control) were not incorporated into the proposed Wet Tropics RAS, it was important
to consider the implications of the putative priorities derived from a review of weeds
present and a preliminary assessment of a 10%+ sample of those. Resources allocated
to the project did not permit the time-consuming assessment of all 504 naturalised
exotic species with a routine assessment estimated at 1-2 days per species (Pheloung
in press:119). Remaining taxa need to be ranked employing the RAS for a
comprehensive regional environmental weed risk assessment. It is only then that
management priorities can be effectively and comprehensively considered. In the
interim, there are some implications for management that do emerge. These are
discussed briefly below.
6.1
The foremost of these implications for management is the importance of ensuring that
potentially invasive plants are not imported for agricultural (particularly pastoral) and
ornamental purposes. Randall (pers. comm.) notes that the numbers of intentionally
introduced plants well outnumber any unintentional introductions, and that more
than 67% of all plant species that have naturalised in Australia over the last 25 or so
years were intentionally introduced for horticultural reasons. This commends as a
highest priority action for any country to put in place a basic system to control
deliberate species importations (Warren pers. comm.), and to strongly urge people
to include screening all new introductions for invasive potential (Randall pers.
comm.).
Despite advances in quarantine screening protocols, very aggressive weeds such as
Leucaena is, and, prior to its elevation to the list of WONS, Hymenachne was, being
actively promoted for pastoral use. Thus, government land management agencies
have provided conflicting advice regarding such plants on the one hand promoting
weed spread and on the other, advising the exclusion of such plants from permitted
import lists, and subsequently for containment and control of these pest species.
Devices such as Memoranda of Understanding (MOUs) and properly constituted
quarantine exclusion systems are required to overcome the cost of control and myopia
(sensu Mooney & Drake 1989:504) practised to date facilitating such importations.
Considerable problems are also posed by the introduction of attractive ornamentals
such as Miconia. The Cairns City Council Pest Management Working Group is
currently aware of a range of other potentially problematic species introductions that
are undertaken for ornamental amenity reasons. These include Triplaris
?surinamensis, the eradication of which is accorded priority in the Citys PMP. Other
ornamentals such as Clerodendrum quadriloculare that are weedy in Micronesia
(Waterhouse pers. comm.) are currently cultivated in the Cairns area and may present
problems if they are permitted to escape.
To a lesser extent some potentially invasive alien species are cultivated and
distributed for food or medicinal properties. Apparently, the proliferation of Mikania
about the Bingil Bay area, and Sweet Prayer Plant (Thaumatococcus daniellii) are
cases in point (Luxton pers. comm.). Waterhouse (pers. comm.) has also noted the
availability of food plants such as Downy Rose Myrtle/Ceylon Hill Cherry
(Rhodomyrtus tomentosa) in nurseries from Rockhampton to Cairns. This plant is
highly problematic in Hawaii and Tahiti and may be another sleeper in this region.
Page 57
Other species that have proved to be invasive within the region such as Allamanda
cathartica, Duranta erecta and Sanchezia parvibracteata continue to be cultivated
and sold by nurseries. In order to combat such problems, a combination of
consultation with the nursery industry (and encouragement of self-regulation) and
sound contributions to wider public wider public awareness campaigns is required.
6.2
Of almost equal importance is instigating control programs where a weed is new, not
widespread and control is feasible (Carter 2000:92). It is vital, therefore, to identify
and control nascent foci (Goodland et al. 1998:12) or incipient invasions of sleeper
weeds ie, plants in initial stages of invasion before their rate of spread is
exponential (Groves 1999) (see Section 5.6).
A number of authors argue strongly for early intervention when incursions are
limited. Braithwaite & Timmins (1999) commend weed surveillance and early
detection to confine weed control to the least cost and that will involve minimal
impact on conservation values. Carter (1999:92) takes a diagrammatic approach to
demonstrate that control is feasible generally only in the early stages of invasion.
Groves (1999:634) demonstrates the cost efficiencies of eradicating new incursions.
Similarly, Panetta (1999:144) argues that, to be effective, weed control actions must
be triggered at low environmental weed densities. Loope (2000:61), in reviewing a
European book on plant invasions, is critical of the authors lack of appreciation of
the importance of rapid response to incipient invasions. The references to weedled control programs of Williams & White (2000:436) further confirm the value of
treatment in early phases of infestation. Earlier, MacDonald et al. (1989:243) warned
that successful control of weeds in nature reserves is uncommon unless control action
is instigated in the earliest phases of the invasion process.
It is instructive to consider management action directed towards species naturalising
in the region considered by Csurhes & Edwards (1998) to be potential (if not actual)
environmental weeds. Six taxa have been identified that are in the initial phase of
invasion and are considered, at this stage, to be amenable to eradication (Table 13).
Table 13: Taxa naturalised in the wet tropics, known to be major weeds elsewhere and
considered susceptible to eradication as they are in the initial phases of establishment (Groves
1999:635; species and assessment of probability of eradication extracted from Csurhes &
Edwards 1998:20-21)
SPECIES
FAMILY
Probability of
eradication
Myrsinaceae
medium
Acanthaceae
Asteraceae
low
low
Miconia calvescens
Melastomataceae
high
Mikania spp.
Thunbergia grandiflora
Asteraceae
Acanthaceae
high
low
CURRENT REGIONAL
DISTRIBUTION
Page 58
The effective control of Panama Rubber (Castilla elastica) by the Cairns City
Councils Pest Management Unit and the Wet Tropics Tree Planting Scheme team is a
case in point. In 1998, incipient infestations of this tree that was originally imported
and maintained at the former Tropical Horticultural Collection of DPI at Kamerunga,
as a producer of a rubber substitute, were noted establishing under the closed canopies
of nearby riparian and adjacent rainforest. Although mainly confined to Kamerunga
Environment Park, the management of which is a joint Cairns City Council and
QPWS responsibility, and on private freehold land, some infestations were also
flourishing in the Barron Gorge National Park section of the World Heritage Area.
This species was afforded highest priority in the Councils Pest Management Plan and
infestations, including 25m tall mature trees, were treated. Currently, follow-up
control is being undertaken by the Pest Management Unit, including searches for
additional seedlings and ongoing monitoring of treated sites, to ensure no resurgence.
The prospects of eradicating this highly invasive alien species from the region are
now very good. This is due to the foresight of the Pest Management Working Group
and the diligence of the Pest Management Unit, the personnel of which understand
that weeds do not respect property lines and do not remain confined awaiting
cumbersome bureaucratic determinations, including resource allocations. They also
recognise that weed control must be timely, transcend tenure boundaries and that
effort will be wasted entirely if there is no follow-up activity.
Particular mention is warranted of the importance (and cost-effectiveness) of strategic
control of incipient infestations of serious weeds such as Miconia calvescens and
Mikania spp., especially in light of the treatment of incursions of Siam Weed, in the
Wet Tropics. This might be extended to several other species. Given its high-risk
rating, the current, relatively restricted distribution of Cucumber Tree suggests that it
is a species that should be targeted for priority control.
6.3
Page 59
Weed control frequently involves removal of target species together with site
disturbance. It has been demonstrated (see Section 2.1) that disturbance facilitates
further alien invasion. It is an ecological reality that reinvasion is more likely to occur
when sites are not occupied. Therefore, weed resurgence is less likely to occur where
sites have been replanted with native species and weed control may need to be
accompanied by revegetation efforts to ensure best results. In the Wet Tropics region,
this is likely to require inter-agency cooperation, for example, between DNR or
Council Pest Management Units and environmental repair teams such as those
operating within the Wet Tropics Tree Planting Scheme.
6.4
Recognition of the serious risks posed by invasive alien species that have established
widespread populations within the area such that eradication is simply not feasible
requires that these be strategically controlled or contained. Control/containment is
primarily required at logistically critical locations in areas that have high conservation
value and/or that contain endandered REs or species. Control may involve local (as
against regional) eradication efforts or judicious containment of, for instance, Par
Grass or Pond Apple infestations adjacent to important wetland reserves.
It is argued that target species for highest priority control should be those rated using
the RAS with scores 50. Some 25 terrestrial taxa (or 30+ species) pose the most
serious environmental risk. These are set out in Table 14.
Table 14: Alien plant taxa adjudged to pose serious environmental risk in the Wet
Tropics region ranked according to risk score (habit codes as in Table 12)
Species
Family
Common name
Annona glabra
Annonaceae
Pond Apple
Habit
Score (%)
TT
90
Leucaena leucocephala
Mimosaceae
Leucaena
Tt
88
Chromolaena odorata
Asteraceae
Siam Weed
SS
82
Sphagneticola trilobata
Asteraceae
Singapore Daisy
82
Hymenachne amplexicaulis
Poaceae
Hymenachne
80
Miconia calvescens
Melastomataceae
Miconia
Tt
80
Psidium guajava
Myrtaceae
Guava
Tt
78
Thunbergia spp.
Acanthaceae
laurel vines
76
Mikania micrantha
Asteraceae
Mile-a-minute
74
Brachiaria mutica
Poaceae
Par Grass
74
Panicum maximum
Poaceae
Guinea Grass
72
Parmentiera aculeata
Bignoniaceae
Cucumber Tree
TT
70
Turbina corymbosa
Convolvulaceae
Turbine Vine
68
Ageratina riparia
Asteraceae
Mistflower
SS
64
Mangifera indica
Anacardiaceae
Mango
TT
64
Eupatorium catarium
Asteraceae
Praxelis
Ss
58
Andropogon gayanus
Poaceae
Gamba Grass
64
Spathodea campanulata
Bignoniaceae
African Tulip
TT
62
Tithonia diversifolia
Asteraceae
Japanese Sunflower
SS
62
Solanum seaforthianum
Solanaceae
Brazilian Nightshade
60
Azadirachta indica
Meliaceae
Neem Tree
Tt
58
Harungana madagascariensis
Clusiaceae
Harungana
TT
56
Stachytarpheta spp.
Verbenaceae
Snakeweeds
Ss
54
Senna obtusifolia
Caesalpiniaceae
Sicklepod
Ss
50
Syngonium podophyllum
Araceae
50
Page 60
6.5
Research Requirements
It is evident also that any effective weed management system must be founded on a
reliable information base. The necessary information is not always in existence,
particularly regarding weed species autecology and even the status of current
distributions of major weed species. To remedy this deficiency research is required in
particular areas. These include:
(i)
(ii)
sensitivity testing of the relative risk ranking obtained using the RAS with the
view to its further refinement;
(iii)
(iv)
(v)
(vi)
Page 61
7.0
Loope (2000:61) reiterates the frequent warning that given time and resistance to
management, invasive plants will undoubtedly contribute to the biological
impoverishment of continents, especially in the areas of significant local endemism,
as is the case in the case of the Wet Tropics Bioregion of north-eastern Queensland.
Therefore, this is not only a serious threat, but also one that cannot be ignored by
authorities, as it will lead to the breaching of Australias international obligations as a
signatory nation to the World Heritage Convention.
The problem of alien invasive species within the context of the Wet Tropics
Bioregion (in particular, management of the World Heritage Area) was considered.
This drew upon an understanding that alien species invasions especially of
environmental weeds - constitute perhaps the second most serious threat to the
survival and integrity of natural systems worldwide. Central also to considerations
was the high conservation significance ascribed to much of the areas vegetation, flora
and fauna and a particular susceptibility of tropical systems and to communities, that
by virtue of their inherent nature, or due to disruption and forest fragmentation, had
become quasi-insular (MacDonald et al.1989:246) in character, rendering them even
more invasion-prone.
An official list of regionally naturalised species obtained from the Queensland
Herbarium was refined to aggregate infraspecific taxa (ie, subspecies/varieties) into a
single taxon, accommodate taxonomic nomenclatural changes and to incorporate at
least 29 species not recorded as naturalised in the collection. These included some of
the regions actually or potentially problematic environmental weeds such as Mikania
micrantha, Schinus terebinthifolia, Hymenachne amplexicaulis, Azadirachta indica
and Pinus caribaea. It is estimated that over 500 exotic species including several
interspecific hybrids have become naturalised in the Wet Tropics Bioregion.
Existing RASs, including some currently being developed, were reviewed and the
most appropriate properties incorporated into a RAS designed explicitly to consider
alien environmental weed risks to the Wet Tropics Bioregion. The RAS specifically
designed to take into account weeds documented for tropical areas, inherent
invasiveness and significance of systems at risk, was proposed and the rationale
underpinning its formulation clarified. Components assessed include gross
invasiveness (ecesis/establishment in native vegetation, to what extent a species is
advantaged by disturbance), a range of intrinsic (biological) attributes predisposing
species to invasiveness (ie, reproductive capacity/mode; dispersal capacity;
competitive ability and ecesis needs) and extrinsic (host environment) factors
(important in the context of World Heritage Area management and regional
ecosystems/species at risk). The latter constitutes the basis for asset-based
management systems that are employed in other states such as Tasmania (Hall 1999)
and South Australia (Virtue 2000) and elsewhere (eg, Hiebert & Stubbendieck 1993).
Incidentally, the Tasmanian system is based on the Exotic Plant Ranking System of
Hiebert & Stubbendieck (1993). Control feasibility, that is frequently incorporated as
a basic element of weed risk assessment systems, was considered secondary from risk
assessment per se. Accordingly, it was treated separately in subsequent management
considerations.
Page 62
This RAS was tested on all seven exotic aquatic species naturalised within the
bioregion and 50 species of terrestrial weeds drawn from a list of 25 derived from
local government Pest Management Plans by DNR (Bebawi, pers. comm.) and
supplemented by 25 other species representative of a range of different weed groups.
Screening of this sample using the new RAS provided plausible results. Notably, the
known worst weeds (eg, Pond Apple and Hymenachne - both WONS together with
Siam Weed, Miconia, Singapore Daisy, Guava, Thunbergia vines and Mikania, that
are known as particularly invasive in other tropical settings) ranked very highly.
Leucaena also ranked the second highest environmental weed risk regionally. It,
along with other deliberately introduced stock forage species such as Par Grass,
Guinea Grass and Gamba Grass, together with pasture legumes, present serious
environmental problems for natural area management. It is argued that urgent
provisions should be made by government and associated pastoral support agencies to
preclude further releases of potentially serious weeds by ensuring observance of the
precautionary principle (see Rozefelds & Mackenzie 1999:583). Therefore, action to
prevent further and continued introduction of highly invasive but considered useful
plants to the region is sorely needed.
Other pertinent management issues are also addressed. These include the urgent need
for a rapid control response to incipient environmental weed incursions, identification
and treatment of sleeper weeds and ecologically integrated control efforts to
instigate containment and reduction of infestations of the worst weeds, especially
those that threaten endangered communities and species. It was also argued that
research is urgently required in some areas and that such research must be regarded as
an intrinsic component of weed management.
Recommendations for further research include peer review and sensitivity testing of
the Wet Tropics RAS and the procurement of additional biological/ecological
information on the 448 naturalised exotics remaining and their assessment using the
RAS. It was also recommended that research also include mapping of infestations
(especially of high scoring weeds with comparatively limited distributions)
throughout the region to assist management deliberations. Lastly, the formulation of a
secondary screening system to explicitly take into account feasibility, costs and
strategic matters associated with weed control and eradication is required urgently if
the serious problem of invasive alien plants is to be addressed effectively within this
and other regions.
Acknowledgments
Special appreciation is extended to Barbara Waterhouse (of AQIS), Des Boorman (of the Nurserymans
Association), Anton vanderSchaan (of SitePlan), Rigel Jensen (of JCU), Andrew Small (of GHD) and to Eric
Higgins (of the Wet Tropics Tree-Planting Scheme, Cardwell Shire) for extremely valuable explicit comments on
exotic species that have naturalised in the region. I am indebted also to Faiz Bebawi, Peter James, Alice Beilby
and Rebecca Hosking of DNR (Land Protection) for facilitating access to some material and to Rachel McFadyen,
Dane Panetta and Vic Little (also of DNR) for their support and useful comments. Gordon Guymer, Peter
Bostock, Bill McDonald and George Batianoff (Queensland Herbarium) were most helpful in providing access to
plant records and for clarifying the taxonomic status of some problematic species. Access to the alien species
Internet chat line - http://indaba.iucn.org/archives/aliens-1/wwwmsgs/ - which is a most useful information source
permitting valuable exchanges with people such as Rod Randall, a Weed Profiler of the Department of
Agriculture, WA, and Paula Warren of the Department of Conservation, NZ - is also gratefully acknowledged.
Page 63
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A1: Page1
A1: Page2
Categorisation
Develop a system that allows discriminate prioritisation of species into categories
applicable to a range of management purposes, such as prevention, eradication,
containment or control
Management Actions
'Management Actions' - Arriving at a 5-year costed program is a logical next stage
(phase 2) of a program once that the desk-top study of weed management
priorities/risk assessment has been completed. For a properly considered 5-year
costed management program to be forthcoming there would need to be more
expansive consultation with Land Protection and related personnel more familiar with
hands-on control techniques, changing availability of control chemicals and
registration protocols, developments in control investigations and distribution and
abundance of target species than is provided for in the current project time frame.
Moreover, there are many unknowables that would militate against this task - for
instance, the continually changing funding sources and conditions for control efforts,
failures to commit to recurrent expenditures that jeopardise initial allocations by not
funding follow-up control efforts, and the generally dynamic nature of weed risk.
In view of these factors it is argued that a 5-year costed program is beyond the scope
of the project at this stage, and instead it may be proposed that once the inventory,
prioritisation and management classification tasks have been completed, a first draft
of a Strategic Action Plan be developed for the WTWHA based on consideration of
control, containment and eradication options.
A1: Page3
Family
Taxon
higher dicots
higher dicots
Acanthaceae
Acanthaceae
Asystasia gangetica
Barleria rosea
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
ferns
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Acanthaceae
Adiantaceae
monocots
higher dicots
monocots
monocots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Agavaceae
Aizoaceae
Alismataceae
Alismataceae
Amaranthaceae
Amaranthaceae
Amaranthaceae
Amaranthaceae
Amaranthaceae
Amaranthaceae
Amaranthaceae
Amaranthaceae
Amaranthaceae
Amaryllidaceae
Anacardiaceae
Anacardiaceae
Anacardiaceae
Anacardiaceae
Barleria strigosa
Brillantaisia lamium
Crossandra infundibuliformis
Hemigraphis alternata
Justicia betonica
Odontonema tubaeforme
Ruellia malacosperma
Sanchezia parvibracteata
Stephanophysum longifolium
Thunbergia alata
Thunbergia grandiflora
Thunbergia laurifolia
Thunbergia mysorensis
Pityrogramma calomelanos var.
calomelanos
Sansevieria trifasciata
Galenia pubescens
Sagittaria graminea
Sagittaria graminea var. platyphylla
Alternanthera bettzickiana
Alternanthera dentata
Alternanthera ficoidea
Alternanthera philoxeroides
Amaranthus hybridus
Amaranthus spinosus
Amaranthus viridis
Celosia argentea
Gomphrena celosioides
Zephyranthes grandiflora
Anacardium occidentale
Harpephyllum caffrum
Mangifera indica
Schinus terebinthifolia
lower dicots
lower dicots
higher dicots
higher dicots
higher dicots
higher dicots
Annonaceae
Annonaceae
Apiaceae
Apocynaceae
Apocynaceae
Apocynaceae
Annona glabra
Annona reticulata
Cyclospermum leptophyllum
Allamanda blanchettii
Allamanda cathartica
Cascabela thevetia
higher dicots
higher dicots
monocots
monocots
monocots
Apocynaceae
Apocynaceae
Araceae
Araceae
Araceae
Catharanthus roseus
Chonemorpha fragrans
Aglaonema commutatum
Colocasia esculenta
Epipremnum aureum
monocots
monocots
Araceae
Arecaceae
Syngonium podophyllum
Syagrus romanzoffiana
lower dicots
lower dicots
lower dicots
higher dicots
higher dicots
higher dicots
Aristolochiaceae
Aristolochiaceae
Aristolochiaceae
Asclepiadaceae
Asclepiadaceae
Asclepiadaceae
Aristolochia elegans
Aristolochia odoratissima
Aristolochia ringens
Asclepias curassavica
Calotropis gigantea
Calotropis procera
Comments
Ornamental (noted to be naturalising by
Boorman, pers. comm.)
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental pondweed
Ornamental pondweed
Ornamental
Fruit tree (Cashew Nut)
Fruit tree
Ornamental naturalising about
Herberton area (pers. obs)
Root stock for fruit tree WONS
Fruit tree (Custard Apple)
Ornamental
Ornamental
Ornamental naturalising in various
places throughout region (pers. obs)
Ornamental
?ornamental
Food plant
Ornamental syn. Scindapsis aurea
listed by Qld Herbarium as doubtfully
naturalised but frequently encourtered
Ornamental
Ornamental invasive of mixed forest
along Priors Ck, Atherton (pers. obs)
Ornamental
Ornamental
Ornamental
?ornamental
A2: Page 1
Category
Family
Taxon
higher dicots
higher dicots
higher dicots
Asclepiadaceae
Asteraceae
Asteraceae
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Gomphocarpus physocarpus
Acanthospermum hispidum
Ageratina riparia (syn. Eupatorium.
riparium)
Ageratum conyzoides subsp. conyzoides
Ageratum houstonianum
Ambrosia artemisiifolia
Arctotheca calendula
Aster subulatus
Bidens alba var. radiata
Bidens pilosa var. pilosa
Carpesium cernuum
Centaurea melitensis
Centratherum punctatum
Chromolaena odorata
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
higher dicots
higher dicots
higher dicots
higher dicots
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Cichorium intybus
Cirsium vulgare
Conyza bonariensis
Conyza canadensis var. canadensis
Conyza canadensis var. pusilla
Conyza leucantha
Conyza sumatrensis
Cosmos caudatus
Crassocephalum crepidioides
Elephantopus mollis
Eleutheranthera ruderalis
Emilia sonchifolia var. javanica
Emilia sonchifolia var. sonchifolia
Erechtites valerianifolia forma valerianifolia
Eupatorium catarium (syn. Praxelis
clematidea)
Galinsoga parviflora
Gamochaeta pensylvanica
Hypochaeris radicata
Mikania micrantha
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Montanoa hibiscifolia
Parthenium hysterophorus
Pseudelephantopus spicatus
Sigesbeckia orientalis
Silybum marianum
Solidago canadensis var. scabra
Sonchus oleraceus
Sphagneticola trilobata
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Asteraceae
Synedrella nodiflora
Tagetes minuta
Tithonia diversifolia
Tithonia rotundifolia
Tridax procumbens
Xanthium occidentale
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Balsaminaceae
Basellaceae
Bignoniaceae
Bignoniaceae
Bignoniaceae
Bignoniaceae
Bixaceae
Boraginaceae
Boraginaceae
Brassicaceae
Brassicaceae
Brassicaceae
Brassicaceae
Brassicaceae
Brassicaceae
Brassicaceae
Impatiens walleriana
Anredera cordifolia
Macfadyena unuis-cati
Parmentiera aculeata
Spathodea campanulata
Tecoma capensis
Bixa orellana
Echium plantagineum
Heliotropium indicum
Brassica juncea
Brassica nigra
Brassica rapa subsp. sylvestris
Cardamine flexuosa
Coronopus didymus
Coronopus integrifolius
Lepidium virginicum
Comments
note nomenclatural change
Bluetop/Billygoat Weed
as above
Ornamental
Ornamental
Brazilian Fireweed
Mistflower note change in taxonomic
nomenclature
Goldenrod
Ornamental bank stabiliser
Singapore Daisy = Wedelia trilobata
Cinderalla weed
Ornamental
Ornamental
Noogoora Burr injurious fruits
= X. pungens
Ornamental
Ornamental
Cats-claw creeper - ornamental
Cucumber Tree = P. edulis
Ornamental
Ornamental
Ornamental honey plant
A2: Page 2
Category
Family
Taxon
Comments
higher dicots
higher dicots
higher dicots
monocots
higher dicots
lower dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Brassicaceae
Brassicaceae
Brassicaceae
Bromeliaceae
Buddlejaceae
Cabombaceae
Cactaceae
Cactaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpiniaceae
Caesalpineaceae
Raphanus raphanistrum
Rorippa palustris
Sisymbrium thellungii
Ananas comosus
Buddleja madagascariensis
Cabomba caroliniana
Opuntia vulgaris
Pereskia aculeata
Bauhinia monandra
Caesalpinia decapetala
Cassia fistula
Cassia grandis
Chamaecrista rotundifolia
Gliricidia sepium
Haematoxylum campechianum
Senna alata
Senna hirsuta
Senna obtusifolia
Senna occidentalis
Senna septemptrionalis
Senna siamea
Senna tora
Sindora supa
Tamarindus indica
Food plant
higher dicots
higher dicots
monocots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
monocots
monocots
monocots
Campanulaceae
Cannabaceae
Cannaceae
Capparaceae
Capparaceae
Capparaceae
Capparaceae
Caprifoliaceae
Caprifoliaceae
Caprifoliaceae
Caricaceae
Caryophyllaceae
Caryophyllaceae
Chenopodiaceae
Clusiaceae
Clusiaceae
Commelinaceae
Commelinaceae
Commelinaceae
Hippobroma longiflora
Cannabis sativa
Canna indica
Cleome aculeata
Cleome gynandra
Cleome hassleriana
Cleome monophylla
Lonicera japonica
Lonicera periclymenum
Sambucus canadensis
Carica papaya
Cerastium vulgare
Stellaria media
Chenopodium ambrosioides
Garcinia xanthchymus
Harungana madagascariensis
Commelina benghalensis
Tradescantia spathacea
Zebrina pendula
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Convolvulaceae
Crassulaceae
Crassulaceae
Cucurbitaceae
Cucurbitaceae
Cucurbitaceae
Cucurbitaceae
Argyreia nervosa
Cuscuta campestris
Ipomoea caraica
Ipomoea hederifolia
Ipomoea indica
Ipomoea nil
Ipomoea obscura
Ipomoea purpurea
Ipomoea quamoclit
Ipomoea triloba
Merremia dissecta
Merremia quinquefolia
Merremia tuberosa
Turbina corymbosa
Bryophyllum daigremontianum
Bryophyllum pinnatum
Coccinia grandis
Cucumis anguria
Cucumis metuliferus
Momordica charantia
higher dicots
monocots
monocots
Cyperaceae
Cyperaceae
Cyperaceae
Cyperus aromaticus
Cyperus brevifolius
Cyperus compressus
Forage legume
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental
Ornamental/drug plant
A2: Page 3
Category
Family
Taxon
monocots
monocots
monocots
monocots
monocots
monocots
monocots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Cyperaceae
Cyperaceae
Cyperaceae
Cyperaceae
Cyperaceae
Cyperaceae
Dioscoreaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Euphorbiaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Cyperus esculentus
Cyperus involucratus
Cyperus metzii
Cyperus rotundus
Cyperus tuberosus
Eleocharis minuta
Dioscorea alata
Acalypha wilkesiana
Chamaesyce hirta
Chamaesyce hyssopifolia
Chamaesyce maculata
Chamaesyce prostrata
Euphorbia cyathophora
Euphorbia heterophylla
Hevea brasiliensis
Jatropha curcas
Jatropha gossypiifolia
Manihot esculenta
Manihot glaziovii
Pedilanthus tithymaloides subsp. smallii
Phyllanthus amarus
Phyllanthus tenellus
Aeschynomene americana
Aeschynomene americana var. americana
Aeschynomene indica
Aeschynomene micranthos
Aeschynomene villosa
Alysicarpus bupleurifolius
Alysicarpus ovalifolius
Alysicarpus vaginalis
Cajanus cajan
Calopogonium mucunoides
Centrosema pascuorum
Centrosema pubescens
Clitoria laurifolia
Clitoria ternatea
Crotalaria goreensis
Crotalaria incana subsp. purpurascens
Crotalaria lanceolata subsp. lanceolata
Crotalaria lunata
Crotalaria ochroleuca
Crotalaria pallida var. obovata
Crotalaria retusa
Crotalaria spectabilis
Crotalaria virgulata subsp. grantiana
Crotalaria zanzibarica
Dalbergia sissoo
Desmodium heterophyllum
Desmodium incanum
Desmodium intortum
Desmodium scorpiurus
Desmodium strigillosum
Desmodium tortuosum
Desmodium uncinatum
Glycine max
Indigofera spicata
Indigofera suffruticosa
Indigofera tinctoria
Inga sp.
higher dicots
higher dicots
higher dicots
Fabaceae
Fabaceae
Fabaceae
Lablab purpureus
Lupinus albus
Macroptilium atropurpureum
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Comments
Food plant
Ornamental
Rubber
Food plant
Food plant
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume (Butterfly Pea)
Ornamental
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
A2: Page 4
Category
Family
Taxon
Comments
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fabaceae
Fagaceae
Flacourtiaceae
Hydrocharitaceae
Pasture legume
Pasture legume
Pasture legume
Pasture legume
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
lower dicots
lower dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lamiaceae
Lauraceae
Lauraceae
Lythraceae
Lythraceae
Malpighiaceae
Malvaceae
Malvaceae
Malvaceae
Malvaceae
Malvaceae
Malvaceae
Malvaceae
Malvaceae
Malvaceae
Malvaceae
Malvaceae
Malvaceae
Marantaceae
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Pasture legume
Ornamental/timber tree (Oak)
Ornamental pondweed recorded only
recently from Mazlin Ck (unpub. data)
Ornamental
Timber tree
Fruit tree
A2: Page 5
Category
Family
Taxon
Comments
higher dicots
higher dicots
higher dicots
Melastomataceae
Melastomataceae
Meliaceae
Miconia calvescens
Tristemma mauritianum var. mauritianum
Azadirachta indica
Ornamental
higher dicots
Meliaceae
Chukrasia velutina
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Mimosaceae
Mimosaceae
Mimosaceae
Mimosaceae
Mimosaceae
Mimosaceae
Mimosaceae
Mimosaceae
Mimosaceae
Mimosaceae
Mimosaceae
Mimoscaeae
Acacia angustissima
Acacia farnesiana
Acacia sinuata
Calliandra surinamensis
Leucaena leucocephala subsp. leucocephala
Mimosa diplotricha var. diplotricha
Mimosa pudica
Mimosa pudica var. hispida
Mimosa pudica var. tetrandra
Mimosa pudica var. unijuga
Samanea saman
Acacia nilotica
higher dicots
higher dicots
Molluginaceae
Moraceae
Mollugo verticillata
Artocarpus ?communis
higher dicots
higher dicots
monocots
higher dicots
Moraceae
Moringaceae
Musaceae
Myrsinaceae
Castilla elastica
Moringa pterygosperma
Musa acuminata x M.balbisiana
Ardisia cf .humilis
higher dicots
higher dicots
higher dicots
higher dicots
Myrsinaceae
Myrsinaceae
Myrsinaceae
Myrtaceae
Ardisia crenata
Ardisia crispa
Ardisia solanacea
Eugenia dombeyi
higher dicots
Myrtaceae
Eugenia uniflora
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
?higher dicots
Myrtaceae
Myrtaceae
Myrtaceae
Oleaceae
Onagraceae
Onagraceae
Oxalidaceae
Oxalidaceae
Passifloraceae
Passifloraceae
Passifloraceae
Passifloraceae
Passifloraceae
Passifloraceae
Passifloraceae
Passifloraceae
Passifloraceae
Passifloraceae
Passifloraceae
Phytolaccaceae
Phytolaccaceae
Pinaceae
Psidium guajava
Psidium guineense
Syzygium cumini
Ligustrum sinense
Ludwigia peploides subsp. montevidensis
Oenothera speciosa
Oxalis corniculata var. corniculata
Oxalis debilis var. corymbosa
Passiflora caerulea
Passiflora coccinea
Passiflora edulis
Passiflora foetida
Passiflora foetida var. foetida
Passiflora foetida var. gossypifolia
Passiflora foetida var. riparia
Passiflora laurifolia
Passiflora quadrangularis
Passiflora suberosa
Passiflora subpeltata
Phytolacca octandra
Rivina humilis
Pinus caribaea
higher dicots
higher dicots
higher dicots
monocots
Piperaceae
Plantaginaceae
Plantaginaceae
Poaceae
Peperomia pellucida
Plantago lanceolata
Plantago major
Andropogon gayanus
monocots
monocots
Poaceae
Poaceae
Ornamental
Pasture legume
now includes M. invisa
Ornamental
a WONS occasionally encountered in
drier parts of region
Jackfruit noted as invasive in Cairns
area by Boorman (pers. comm.)
Provides rubber substitute
Fruit-bearing plant
Ornamental - if A. humilis it is a major
weed elsewhere but may be confused
with A. solanacea (see below Hyland
& Waterhouse pers. comm.)
Ornamental
Ornamental
Ornamental
Fruit-bearing plant noted naturalising
by Stanton (peres. comm.)
Fruit-bearing plant recorded in intact
native vegetation at various locations
(eg, Cardwell see Werren 1998)
Fruit tree
?fruit tree
Fruit tree (Java Plum)
Ornamental
Ornamental
Fruit-bearing plant
?ornamental
Timber tree wildings extensively
established around numerous
plantations (pers. obs)
A2: Page 6
Category
Family
Taxon
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Axonopus fissifolius
Bambusa vulgaris
Bothriochloa insculpta
Brachiaria brizantha
Brachiaria decumbens Stapf
Brachiaria decumbens Stapf cv Basilisk
Brachiaria humidicola
Brachiaria mutica
Cenchrus caliculatus
Cenchrus ciliaris
Cenchrus echinatus
Cenchrus setiger
Chloris gayana
Chloris inflata
Chloris virgata
Cynodon aethiopicus
Cynodon nlemfuensis var. nlemfuensis
Cyrtococcum deltoideum
Dactyloctenium aegyptium
Dactyloctenium australe
Dichanthium annulatum
Dichanthium aristatum
Dichanthium caricosum
Digitaria ciliaris
Digitaria didactyla
Digitaria eriantha
Digitaria violascens
Echinochloa colona
Echinochloa crus-galli
Echinochloa frumentacea
Echinochloa polystachya
Echinochloa polystachya cv. Amity
Eleusine indica
Eragrostis amabilis
Eragrostis cilianensis
Eragrostis minor
Eragrostis pilosa
Eragrostis subsecunda
Eragrostis tenuifolia
Eriochloa meyeriana
Eustachys distichophylla
Hordeum vulgare subsp. Vulgare
Hymenachne amplexicaulis
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Hyparrhenia hirta
Hyparrhenia rufa
Hyparrhenia rufa subsp. altissima
Hyparrhenia rufa subsp. rufa
Lolium perenne
Lolium x hubbardii
Lolium x hybridum
Melinis minutiflora
Melinis repens
Panicum coloratum
Panicum maximum var. coloratum
Panicum maximum var. maximum
Panicum maximum var. maximum cv
Coloniao
Panicum maximum var. maximum cv. Hamil
Panicum maximum var. trichoglume
Paspalum conjugatum
Paspalum dilatatum
Paspalum notatum
Paspalum paniculatum
Paspalum plicatulum
Paspalum urvillei
Paspalum virgatum
Comments
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture (ponded) grass (Para Grass)
Pasture grass
Pasture grass (Buffel Grass)
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass (Guinea Grass)
Pasture grass
Pasture grass (Hamel Grass)
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass (Clyde River Grass)
A2: Page 7
Category
Family
Taxon
Comments
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Paspalum wettsteinii
Pennisetum alopecuroides
Pennisetum clandestinum
Pennisetum glaucum
Pennisetum pedicellatum subsp. unispiculum
Pennisetum purpureum
Phalaris canariensis
Phalaris minor
Phyllostachys bambusoides
Poa annua
Saccharum officinarum
Saccharum spontaneum
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
monocots
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
Poaceae
monocots
monocots
monocots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Poaceae
Poaceae
Poaceae
Polygalaceae
Polygonaceae
Polygonaceae
Polygonaceae
Polygonaceae
Themeda quadrivalvis
Urochloa mosambicus
Zea mexicana
Polygala paniculata
Acetosella vulgaris
Emex australis
Fallopia convolvulus
Triplaris americana/surinamensis
monocots
higher dicots
higher dicots
ferns
higher dicots
higher dicots
higher dicots
higher dicots
Pontederiaceae
Portulacaceae
Primulaceae
Pteridaceae
Rhamnaceae
Rosaceae
Rubiaceae
Rubiaceae
Eichhornia crassipes
Talinum paniculatum
Anagallis pumila
Pteris semipinnata
Ziziphus mauritiana
Rubus alceifolius
Coffea arabica
Coffea liberica
higher dicots
higher dicots
Rubiaceae
Rubiaceae
Mitracarpus hirtus
Musenda frondosa
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
Rubiaceae
Rubiaceae
Rubiaceae
Rubiaceae
Rubiaceae
Rutaceae
Rutaceae
Rutaceae
Rutaceae
ferns
higher dicots
Salviniaceae
Sapindaceae
Salvinia molesta
Blighia sapida
higher dicots
higher dicots
Sapindaceae
Sapindaceae
higher dicots
Sapotaceae
Cardiospermum halicacabum
Cardiospermum halicacabum var.
halicacabum
Chrysophyllum cainito
Ornamental + other
food plant (Sugar Cane)
listed as doubtfully naturalised by Qld
Herbarium but known locally to be
somewhat invasive (pers. obs)
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Pasture grass
Ornamental
Food plant (Chinee Apple)
Food plant
Food plant -listed as doubtfully
naturalised by Qld Herbarium but
recored as naturalising (Stanton, pers.
comm, Boorman, Pers. comm.)
shrubby garden escapee along
powerline corridor on the approaches to
Bramston Beach (Jensen, pers. comm.)
Fruiy-bearing tree
Fruiy-bearing tree (Lemon)
Food plant (curry leaf)
Ornamental inclusive of M.paniculata
cv. exotica
Ornamental aquatic
Fruit-bearing tree naturalising along
creek banks and forest edges along
footslopes of the McAlister Range west
of Palm Cove (Small, pers. comm.)
A2: Page 8
Category
Family
Taxon
higher dicots
higher dicots
Scrophulariaceae
Scrophulariaceae
Angelonia salicariifolia
Lophospermum erubescens
higher dicots
higher dicots
spike mosses
spike mosses
spike mosses
spike mosses
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
higher dicots
monocots
monocots
monocots
monocots
Scrophulariaceae
Scrophulariaceae
Selaginellaceae
Selaginellaceae
Selaginellaceae
Selaginellaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Solanaceae
Theaceae
Tiliaceae
Tiliaceae
Tiliaceae
Urticaceae
Urticaceae
Verbenaceae
Verbenaceae
Verbenaceae
Verbenaceae
Verbenaceae
Verbenaceae
Verbenaceae
Verbenaceae
Verbenaceae
Verbenaceae
Zingiberaceae
Zingiberaceae
Zingiberaceae
Zingiberaceae
Mecardonia procumbens
Scoparia dulcis
Selaginella plana
Selaginella umbrosa
Selaginella vogelii
Selaginella wildenovii
Brugmansia x candida
Capsicum annuum var. glabriusculum
Capsicum frutescens
Datura stramonium
Lycium barbarum
Lycopersicon esculentum
Nicandra physalodes
Nicotiana glauca
Physalis peruviana
Solanum capsicoides
Solanum erianthum
Solanum mauritianum
Solanum nigrum
Solanum pseudocapsicum
Solanum seaforthianum
Solanum torvum
Camellia sinensis
Muntingia calabura
Triumfetta pilosa
Triumfetta rhomboidea
Boehmeria nivea
Pilea microphylla
Duranta erecta
Lantana camara var. camara
Lantana montevidensis
Stachytarpheta cayennensis
Stachytarpheta jamaicensis
Stachytarpheta mutabilis
Stachytarpheta x adulterina
Stachytarpheta x trimenii
Verbena incompta
Verbena litoralis
Alpinia zerumbet
Costus dubius
Hedychium coronarium
Zingiber officinale
Comments
Rampant along road verges of Maalan
circuit (Jensen, pers. comm.) and along
the Beatrice (Small, pers. comm.)
Ornamental
Ornamental
Ornamental
Ornamental
Fruit-bearing plant
Fruit-bearing plant
Ornamental
Fruit-bearing plant
Drug plant
Fruit-bearing plant
Ornamental
Food (beverage) plant
Fruit tree
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